Parker Waichman LLP
‘No Record’ Of Letters, Prosecutors Say
Attorney’s office has found no evidence of Abuse. An “exhaustive” search by the city state’s attorney’s office has found no evidence it was informed by the Archdiocese Of Baltimore in 1998 of allegations that the Rev. Maurice J. Blackwell had had sex with a boy decades earlier, a spokeswoman said yesterday. “Our office can say … [Read more...] about ‘No Record’ Of Letters, Prosecutors Say
Journal Says Church Aware Of Sex Abuse
Archdiocese Was Well Aware Of Sex Abuse. A journal kept by a priest who struggled against his sexual attraction to children indicates the archdiocese was well aware of the problem long ago and chose to deal with it in private. The 246-page journal was kept by the Rev. Louis E. Miller, who underwent 12 years of therapy to deal with … [Read more...] about Journal Says Church Aware Of Sex Abuse
New Claims Brought Against Juneau Priest
Claims Brought Against Juneau Priest. More accusations of inappropriate behavior have been made against a Juneau Catholic priest accused last fall of sexual abuse, the Juneau diocese said. The new claims made against the Rev. Michael Nash will be forwarded to a Vatican committee, which will decide his future in the … [Read more...] about New Claims Brought Against Juneau Priest
Molestation Charge Is Filed Nine Years After Alleged Incident
Age of Child Allows Prosecutors More Time On Molestation Charge. It may be the first time in St. Clair County that a criminal sexual assault has been charged over nine years after the crime happened. Arciles “A.J.” Lucas Jr., 37, faces aggravated criminal sexual assault charges and criminal sexual assault charges for molesting a … [Read more...] about Molestation Charge Is Filed Nine Years After Alleged Incident
Black Decker Recalls Electric BlowerVacuumMulchers Due to Faulty Fan Cover
Black Decker Recalls Over Faulty Fan Cover. A recall is being issued for Black & Decker electric blower/vacuum/mulchers due to a laceration hazard. The problem stems from the fact that the fan cover can unlatch unexpectedly, causing injuries. Townson, Maryland-based Black & Deck is recalling about 560,000 units sold … [Read more...] about Black Decker Recalls Electric BlowerVacuumMulchers Due to Faulty Fan Cover
Lawsuits Filed Over Samsung’s Galaxy Note7 Exploding Hazard
Samsung's Galaxy Note7 Exploding Hazard. Samsung Electronics Co. Ltd., the world's largest smartphone manufacturer, is facing another lawsuit over the allegedly exploding Galaxy Note7. The South Korean company now faces a product liability lawsuit after a Galaxy S7 Edge exploded in a man's back pocket while he was … [Read more...] about Lawsuits Filed Over Samsung’s Galaxy Note7 Exploding Hazard
Massachusetts Appeals Court Returns Transvaginal Mesh Case to Court for Reconsideration
Massachusetts Appeals To The Transvaginal Mesh Case To Be Reheard. More than two years, a jury in a Boston Scientific transvaginal mesh trial found in favor of the manufacturer. The plaintiff appealed the verdict, and the Massachusetts Appeals Court has recently agreed with the plaintiff, and the case will be … [Read more...] about Massachusetts Appeals Court Returns Transvaginal Mesh Case to Court for Reconsideration
Samsung Should Have Notified CPSC of Galaxy Note 7 Recall
The CPSC Is Criticizing Samsung Over Its Recall. The Consumer Product Safety Commission (CPSC) is criticizing the way Samsung handled its recall of the Galaxy Note 7. The newly released phone poses a fire hazard because of its defective lithium-ion battery, which can overheat and explode. Samsung, based in South Korea, … [Read more...] about Samsung Should Have Notified CPSC of Galaxy Note 7 Recall
Babyganics Lawsuit Brought Over Misleading Business Practice Allegations
Babyganics Has Been Accused In A Lawsuit. KAS Direct LLC, which also does business as Babyganics, has been accused in a recently filed class action lawsuit of touting its baby products as organic, despite the products are chemical based. The case has been filed in the U.S. District Court for the Southern District of New … [Read more...] about Babyganics Lawsuit Brought Over Misleading Business Practice Allegations
Ravioli Recalled due to Plastic Pieces Found in Product
Ravioli Recalled Due To Plastic Contamination. The supermarket chain Wegmans recalled ravioli due to white plastic pieces reportedly found in a particular product. The recalled ravioli is Wegmans Italian Classics Striped Ricotta & Spinach Ravioli, 9- ounce, UPC # 0-77890-38934, sold between August 2 and August 30, 2016. … [Read more...] about Ravioli Recalled due to Plastic Pieces Found in Product
New Biomet Metal on Metal Hip Implant Lawsuit
Lawsuit Filed Against Biomet After Hip Surgery. A woman from New York had a Biomet M2a Magnum Hip Replacement System implanted six years ago. The 61-year-old has filed a lawsuit against the manufacturer alleging the device has caused her severe injury. As a result of her hip surgery, the woman has experienced constant … [Read more...] about New Biomet Metal on Metal Hip Implant Lawsuit
Another Lawsuit Brought Against Johnson Johnson Ethicon Over Pelvic Mesh Injuries
Lawsuit Against Johnson Johnson Ethicon Pelvic Mesh Injuries. A civil lawsuit brought against Johnson & Johnson, as well as its medical device unit, Ethicon, includes allegations that Johnson & Johnson and Ethicon used deceptive marketing over its surgical transvaginal mesh. Litigation over pelvic mesh devices continues to … [Read more...] about Another Lawsuit Brought Against Johnson Johnson Ethicon Over Pelvic Mesh Injuries
Court Ruling May Pave the Way for More Essure Lawsuits
Court Ruling for Essure Lawsuits. Essure lawsuits are already underway, and a recent court ruling could fuel even more cases. Women across the country are filing lawsuits alleging that Essure, a sterilization device manufactured by Bayer, led to injuries such as severe pain and organ perforation. In Missouri, a lawsuit was … [Read more...] about Court Ruling May Pave the Way for More Essure Lawsuits
Mounting Lawsuits Allege Monsanto’s Roundup Caused Cancer
Monsanto's Roundup Herbicide Causes Cancer. Monsanto is facing a number of lawsuits alleging that an ingredient in its Roundup herbicide causes cancer. According to the Madison Record, growing litigation in Illinois could turn into a class action lawsuit against Monsanto Co., a multinational agrochemical manufacturer. Lawsuits have … [Read more...] about Mounting Lawsuits Allege Monsanto’s Roundup Caused Cancer
What Complications may Result from Inferior Vena Cava (IVC) Filters?
Lawsuits Over IVC Filters. The number of lawsuits over inferior vena cava filters continues to rise, with over 1,500 cases filed, according to court records. IVC filters are umbrella-shaped devices placed in the inferior vena cava to prevent blood clots from reaching the lungs. Lawsuits filed over the devices allege that … [Read more...] about What Complications may Result from Inferior Vena Cava (IVC) Filters?
Victims of Transvaginal Mesh Complications Doubt FDA
Woman Who Experienced Transvaginal Mesh Complications Questioned FDA. Research published in Obstetrics and Gynecology on May 4, 2016 by Northwestern University criticizes the agency for approving a number of high-risk women's health devices based on weak clinical studies, including transvaginal mesh. Lead researcher Dr. … [Read more...] about Victims of Transvaginal Mesh Complications Doubt FDA
Controversy Over Power Morcellator Use in Hysterectomy Procedures
Woman Seeking Legal Action Against Power Morcellator for The Spread of Cancer. A number of women are coming forward seeking legal action after they have been diagnosed with uterine cancer, blaming the power morcellator for the spread of their disease. The women hold the manufacturers of the devices responsible for being negligent in … [Read more...] about Controversy Over Power Morcellator Use in Hysterectomy Procedures
Talcum Powder and Uterine Cancer Linked in JJ Lawsuit
another talcum powder lawsuit has been filed against J&J Another Talcum Powder Lawsuit Filed Against J&J. In the U.S. District Court for the Northern District of California, another talcum powder lawsuit has been filed against Johnson & Johnson (J&J). The plaintiff alleges that after using J&J's Baby Powder … [Read more...] about Talcum Powder and Uterine Cancer Linked in JJ Lawsuit
Multidistrict Litigation for Talcum Powder Ovarian Cancer Cases Petitioned by Plaintiff
A talcum powder lawsuit to centralize all ovarian cancer lawsuits into a MDL Ovarian Cancer Cases Into A Multidistrict Litigation. The U.S. Judicial Panel on Multidistrict Litigation has been petitioned by a plaintiff in a talcum powder lawsuit to centralize all ovarian cancer lawsuits into a multidistrict litigation (MDL). … [Read more...] about Multidistrict Litigation for Talcum Powder Ovarian Cancer Cases Petitioned by Plaintiff
Kimberly-Clark and Halyard Health Face Class Action Filed Over Defective Surgical Gowns
Lawsuit on Halyard Health and Kimberly Clark Corporation Over Surgical Gowns. Halyard Health and Kimberly-Clark Corporation have been hit with a class action lawsuit on behalf of people who purchased or otherwise acquired Kimberly-Clark and Halyard securities from February 2013 through April 2016. The class action, filed in United … [Read more...] about Kimberly-Clark and Halyard Health Face Class Action Filed Over Defective Surgical Gowns
Cook Medical IVC Filter Plaintiffs Hope for Settlement before September Trials
IVC Filter Plaintiffs Settlement Conference Scheduled Postponed. In the multidistrict litigation (MDL) involving Cook Medical IVC blood clot filters, plaintiffs and their attorneys hope that a settlement can be reached before cases come to trial in September 2016. A settlement conference originally scheduled for March 2016 was … [Read more...] about Cook Medical IVC Filter Plaintiffs Hope for Settlement before September Trials
Judge Rachelle Harz Takes over Mirena IUD Litigation in NJ
Mirena IUD Litigation Holds By The New Judge. A new judge is overseeing the Mirena IUD multicounty litigation in Bergen County, New Jersey. Court documents indicate that Judge Brian Martinotti, who has presided over proceedings up until this point, will be leaving the Bergen County bench to assume new duties in Federal … [Read more...] about Judge Rachelle Harz Takes over Mirena IUD Litigation in NJ
Bard IVC Filter Litigation in Bellwether Selection Phase
Cases Selected in Bard IVC Filter Selection Process. The U.S. Judicial Panel on Multidistrict Litigation (JPML) consolidated all federally filed C.R. Bard interior vena cava (IVC) filter lawsuits into one court in the District of Arizona in August 2015. Since, both sides have been working on bellwether case … [Read more...] about Bard IVC Filter Litigation in Bellwether Selection Phase
Talcum Powder Ovarian Cancer Trial Scheduled for Early February 2017
A consolidated litigation underway in federal court in Missouri. Talcum Powder Lawsuits Continue To Move Forward. Hundreds of talcum powder ovarian cancer lawsuits continue to move toward trial in a consolidated litigation underway in federal court in Missouri. A pretrial order issued on June 20, 2016 changed a trial starting … [Read more...] about Talcum Powder Ovarian Cancer Trial Scheduled for Early February 2017
Johnson Johnson Sued by over 1000 Women for Alleged Cover Up of Talc Cancer Risk
J&J Was Negligent For Talc Cancer Risk. A lawsuit against Johnson & Johnson (J&J) claiming the company was negligent in providing information about risks of ovarian cancer has been joined by over 1,000 women. Imerys Talc America, the largest talc supplier in America and the only source of talc for J&J is … [Read more...] about Johnson Johnson Sued by over 1000 Women for Alleged Cover Up of Talc Cancer Risk
Skincare Company gets FDA Warning Letter
Skincare Company Selling Unapproved Drugs. A warning letter was issued by the U.S. Food and Drug Administration (FDA) to a skincare company for promoting and selling unapproved new drugs. Whether at the District Office level or at Headquarters, the FDA will take steps against products promoted with unproven claims about a … [Read more...] about Skincare Company gets FDA Warning Letter
India Child Protection Agency wants JJ Baby Products Tested for Hazardous Chemicals
Safety Of JJ Baby Products. A recent verdict awarded $72 million to the family of a woman who died of ovarian cancer, allegedly due to using Johnson & Johnson's talcum powder for feminine hygiene. That award, along with the talcum powder litigation in general, has sparked questions about the safety of talcum-based and other … [Read more...] about India Child Protection Agency wants JJ Baby Products Tested for Hazardous Chemicals
Spray Tanners Can Cause Breathing Problems
Breathing Problems Associated With Spray Tanners. A young British woman developed serious breathing problems after she applied a spray-on tanner, though the product had been recalled nearly three years ago. Moments after Lucy Fowler sprayed St. Tropez Instant Wash Off Face and Body Spray, an aerosol bronzing mist on her … [Read more...] about Spray Tanners Can Cause Breathing Problems
Complications with IVC Filters are Evaluated
Evaluation of IVC Filters Complications. Inferior vena cava (IVC) filters are cage-like devices built to catch and dissolve blood clots. They are inserted in patients who have an increased risk of blood clots, but for whom blood thinners may not be an option. An IVC filter works by trapping blood clots before they can … [Read more...] about Complications with IVC Filters are Evaluated
Dometic RV and Boat Refrigerators Dangerous Defects
Lawsuit Against Dometic Over Dangerous Defects Of Its Product. A class action lawsuit is being brought against Dometic Corporation, manufacturer of gas absorption refrigerators for boats and RVs. The complaint alleges that "the refrigerators contain dangerous defects that can cause them to vent pressurized hydrogen and … [Read more...] about Dometic RV and Boat Refrigerators Dangerous Defects
$46.5M Awarded by Jury in Most Recent PCB Lawsuit
Punitive Damages Over PCB Lawsuit. A St. Louis jury awarded $46.5 million to plaintiffs in a month-long trial that began April 28. The jury voted awarded $17.5 million in damages and $29 million in punitive damages against Monsanto alleging negligence in the production of PCBs. The plaintiffs claimed exposure to polychlorinated … [Read more...] about $46.5M Awarded by Jury in Most Recent PCB Lawsuit
Failed Retrieval of Optional Inferior Vena Cava Filters
Concerns for Inferior Vena Cava Filters Retrievals. A retrievable inferior vena cava filter (IVC) is a small, metal device made to stop a blood clot from traveling to the lungs. The device resembles a metal cage and is surgically inserted into a patient’s inferior vena cava, which is the vein that takes blood back to the heart and … [Read more...] about Failed Retrieval of Optional Inferior Vena Cava Filters
J&J Ordered to Pay $55 Million in Missouri Talcum Powder Trial
J&J has been ordered to pay $55 million to a plaintiff in a trial in Missouri. J&J Pay To A Plaintiff In A Talcum Powder Trial. Johnson & Johnson (J&J) has been ordered to pay $55 million to a plaintiff in a trial in Missouri. The plaintiff contracted ovarian cancer allegedly as a result of using J&J talcum … [Read more...] about J&J Ordered to Pay $55 Million in Missouri Talcum Powder Trial
Boston Scientific Recalls Catheter FDA Panel to Vote on Clovis Cancer Drug
Recall for Boston Scientific's Fetch 2 Aspiration Catheter. A Class I recall has been issued for Boston Scientific's Fetch 2 Aspiration Catheter, due to the risk of shaft breakage during surgery. The device is used to remove small blood clots from coronary arteries. Class I recalls are the FDA's most serious type of recall; … [Read more...] about Boston Scientific Recalls Catheter FDA Panel to Vote on Clovis Cancer Drug
Feds Convene Grand Jury in Boston Scientific Transvaginal Mesh Investigation
Transvaginal Mesh Investigation Alleging Boston Scientific Schemed to Make Counterfeit Materials For Pelvic Mesh Devices. According to Mass Device, a grand jury has been impaneled in a case alleging Boston Scientific schemed to produce counterfeit materials for its pelvic mesh products. The federal government and the U.S. … [Read more...] about Feds Convene Grand Jury in Boston Scientific Transvaginal Mesh Investigation
Boston Scientific Investigated by FDA for Alleged Counterfeit Raw Materials in Vaginal Mesh Implants
FDA Examining Allegation That Boston Scientific Corp. Used Smuggled Materials. The U.S. Food and Drug Administration (FDA) is examining allegations that Boston Scientific Corp. used counterfeit raw materials smuggled from China to use in vaginal mesh implants. The mesh implants are used to treat urinary incontinence and various … [Read more...] about Boston Scientific Investigated by FDA for Alleged Counterfeit Raw Materials in Vaginal Mesh Implants
Zimmer Biomet Hips Recalled for Contamination
Contamination in Zimmer Biomet Hips Device. Zimmer Biomet recalled the M/L Taper Femoral Stem and Neck hip replacement system with Kinectiv Technology after discovering the devices are contaminated with residues from the manufacturing process. The residues on the Zimmer hip components can cause serious health issues … [Read more...] about Zimmer Biomet Hips Recalled for Contamination
Intra-Aortic Balloon Catheters and Insertion Kits Recalled: Sheath Body May Separate from Hub
Intra-Aortic Balloon Catheters Recalled. Teleflex Incorporated has announced a worldwide recall of Arrow International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits. Teleflex initiated the recall in February, 2016 for 47,140 units distributed to hospitals, clinics, and medical centers throughout the … [Read more...] about Intra-Aortic Balloon Catheters and Insertion Kits Recalled: Sheath Body May Separate from Hub
Splenda Artificial Sweetener Linked to Higher Risk of Leukemia
Link Between Risk OF Leukemia And Splenda Artificial Sweetener. A study published in the International Journal of Occupational and Environmental Health links the artificial sweetener Splenda to an increased risk of leukemia. Splenda, otherwise known as sucralose, was introduced in 1999. It has been marketed as an … [Read more...] about Splenda Artificial Sweetener Linked to Higher Risk of Leukemia
DePuy Pinnacle Bellwether Trial Goes to the Jury
DePuy Pinnacle Trials Goes To The Jury. Testimony has finished in the bellwether trial involving the DePuy Orthopaedics Pinnacle metal on metal hip implant, and the case has gone to the jury. The outcome of this case could be for the disposition of a number of pending cases. The five plaintiffs in the case allege the Pinnacle hip … [Read more...] about DePuy Pinnacle Bellwether Trial Goes to the Jury
Patients with IVC Filters Examined for Thrombosis
Study Found Unretrieved IVC Filters Caused Blood Clots. A recent study published in JACC (Journal of American College of Cardiology) Cardiovascular Interventions reveals that unretrieved inferior vena cava (IVC) filters are often the cause of blood clots. "Due to the substantial increase in the number of IVC filters placed in the … [Read more...] about Patients with IVC Filters Examined for Thrombosis
Consumers Sue Over Allergies and Skin Reactions to Just for Men Hair Dye Products
Suit Against The Manufacturer Of Just for Men Hair Dye. A group of consumers is seeking Certification for a class action suit against the manufacturer of Just for Men hair dye. The consumers told a Missouri federal court last week that the manufacturer did not warn consumers about burns and severe allergies they could … [Read more...] about Consumers Sue Over Allergies and Skin Reactions to Just for Men Hair Dye Products
Center for Auto Safety Calls Jeep Gas Tank Fires the Most Lethal Vehicle Safety Issue
Jeep Gas Tank Defect Is The Most Lethal. According to Clarence Ditlow, executive director of the nonprofit Center for Auto Safety, the Takata airbag inflator defect is not the most lethal vehicle safety issue. Ditlow says the major safety issue is "the fuel tank behind the rear axle in the 1993-98 Jeep Grand Cherokee, … [Read more...] about Center for Auto Safety Calls Jeep Gas Tank Fires the Most Lethal Vehicle Safety Issue
After Tenth Death Takata Airbag Recall Expanded
Takata Airbag Could Explode. Honda Motor Co. has added another 2.23 million vehicles in the U.S. to the list of vehicles recalled over Takata airbags that could explode. On Wednesday, February 2, the automaker said that Honda and Acura vehicles from the 2005 to 2016 model years will have Takata-manufactured driver-side … [Read more...] about After Tenth Death Takata Airbag Recall Expanded
Federal Judge Denies Claim of Preemption in Zofran Birth Defect Litigation
Zofran May Cause Birth Defects. U.S. District Judge F. Dennis Saylor IV has denied GlaxoSmithKline's motion to dismiss all claims in multidistrict litigation alleging that the company's off-label promotion of its anti-nausea drug Zofran (ondansetron) for morning sickness led to birth defects. Judge Saylor denied the … [Read more...] about Federal Judge Denies Claim of Preemption in Zofran Birth Defect Litigation
Monsanto Seeks to Block Carcinogenic Designation for Roundup
Roundup Chemicals Known To Cause Cancer. Monsanto Corporation has filed a lawsuit to block the California Office of Environmental Health Hazard Assessment (OEHHA) from adding glyphosate-the main ingredient in Roundup-to its listing of chemicals known to cause cancer. The list of chemicals is authorized under California's … [Read more...] about Monsanto Seeks to Block Carcinogenic Designation for Roundup
Wegmans Food Markets Must Recall Chicken Products
Wegmans Food Recall Chicken Products. On January 5, 2016 the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced that Wegmans Food Markets Inc. was recalling approximately 1,125 pounds of chicken products that were produced without required federal inspection. The uninspected chicken products were … [Read more...] about Wegmans Food Markets Must Recall Chicken Products
Medtronic Uses Preemption in Medtronic Infuse Case, Again
US Supreme Court Denied the Case of Medtronic.The denial of review by the United States Supreme Court today in the case of Caplinger v. Medtronic, Inc., Docket No. 15-321, though it might appear to be a victory for medical device manufacturer, Medtronic, Inc., it was not. While a shallow analysis of the Supreme Court’s action in … [Read more...] about Medtronic Uses Preemption in Medtronic Infuse Case, Again
Second Lawsuit Against Ikea Within a Year over Childs Death in Dresser Tip-over
Injuries Caused By A Dresser Tip-Over. A second lawsuit has been filed in a year over a child's death from injuries caused by an Ikea dresser that tipped over on the child. Parents of a Washington state toddler fatally injured in an Ikea dresser tip-over over have filed a lawsuit against the Swedish furniture retailer in the … [Read more...] about Second Lawsuit Against Ikea Within a Year over Childs Death in Dresser Tip-over
Congressman Seeks Criminal Inquiry into Morcellator Deaths
Congressman Calling Office of Crminal Investigation to Investigate Morcellator Deaths. Pennsylvania Congressman Michael Fitzpatrick is calling on the U.S. Food and Drug Administration's (FDA's) Office of Criminal Investigations to investigate three deaths associated with the use of power morcellators, Qmed reports. Morcellators are … [Read more...] about Congressman Seeks Criminal Inquiry into Morcellator Deaths
Death of High School Football Player Sparks Lawsuit
The Parents A Football Player Died, Filed A Lawsuit. The parents of a 16-year-old New York City high school football player who collapsed during a 2014 football practice and later died have filed a wrongful death lawsuit. In court papers filed in December 2015, the parents allege that the city, education officials, and … [Read more...] about Death of High School Football Player Sparks Lawsuit
Research Study Warns about Adverse Effects of NSAIDs on Ovulation
NSAIDs May Adversely Affect Ovulation. A presentation at the 2015 European League Against Rheumatism (EULAR) Annual Congress, researchers warned that nonsteroidal anti-inflammatory drugs (NSAIDs) may adversely affect ovulation. NSAIDs are among the most commonly prescribed drugs for pain and inflammation and are frequently used by … [Read more...] about Research Study Warns about Adverse Effects of NSAIDs on Ovulation
Parents Beware: Your Children’s New Holiday Toys May be Dangerous
Holiday Toys May Put The Child At Risk For Injury. With the holidays just ending, millions of children are happily playing with wished-for toys showered on them by parents and grandparents. But many toys, intended to bring hours of pleasure, may instead put the child at risk for injury or, in the worst cases, … [Read more...] about Parents Beware: Your Children’s New Holiday Toys May be Dangerous
Kentucky Reaches $39.5 Million Settlement in OxyContin and Risperdal Suits
Purdue Pharma LP and Johnson & Johnson will pay a combined $39.5 million to settle lawsuits brought by the state of Kentucky over the narcotic OxyContin and antipsychotic Risperdal, the state attorney general said. Under the terms of the settlements-which end nearly nine years of litigation-Purdue will pay $24 million to the … [Read more...] about Kentucky Reaches $39.5 Million Settlement in OxyContin and Risperdal Suits
Consumers Often Surprised with Unexpected Charges for Wear and Damage at End of Auto Lease
Consumers Opting Auto Lease Rather Than Purchasing. Many consumers are opting to lease new or used motor vehicles rather than purchase them outright. Consumers rented more than one out of every four new vehicles and that figure has risen significantly in the past two years-some 27 percent, from 22 percent in 2012-Edmunds … [Read more...] about Consumers Often Surprised with Unexpected Charges for Wear and Damage at End of Auto Lease
Consumers Can Sue Over Organic Food Mislabeling
Supreme Court Supports Consumers Over Organic Food Mislabeling.An unprecedented decision by the California Supreme Court supports the rights of consumers to sue over the mislabeling of organic food. In a case against Herb Thyme Farms, Inc., the high court unanimously ruled that consumers can file a lawsuit against growers who … [Read more...] about Consumers Can Sue Over Organic Food Mislabeling
Off-Label Lawsuit is Not Barred by Texas Tort Reforms Court Rules
Off-Label Lawsuit is Not Barred. The Third Court of Appeals in Austin has ruled that an off-label lawsuit is not barred by Texas tort reforms, Law 360 reports. The court found that the lawsuit, which accuses manufacturer Verticor Ltd. of paying kickbacks for off-label use of a medical device, is not subject to the same rules the … [Read more...] about Off-Label Lawsuit is Not Barred by Texas Tort Reforms Court Rules
FDA Issues Safety Alert on Underactive Thyroid in Infants
The U.S. Food and Drug Administration (FDA) has issued a safety alert noting that "rare cases of underactive thyroid have been reported in infants following the use of contrast media containing iodine, also called 'contrast dye,' for X-rays and other medical imaging procedures." This problem has been the subject of investigation … [Read more...] about FDA Issues Safety Alert on Underactive Thyroid in Infants
General Motors Recalls 1.4M Cars for Engine Fire Risk
General Motors Recalled Older Cars. General Motors has recalled 1.4 million older cars for a repair to prevent engine fires. This is the second recall for some of the cars. At least 1,345 cars have caught fire even after the first repair. GM has acknowledged that the repair did not work, the Associated Press (AP) reports. In some … [Read more...] about General Motors Recalls 1.4M Cars for Engine Fire Risk
Two Cookie Varieties from Tate’s Bake Shop Recalled for Undeclared Walnuts
Tate’s Bake Shop Cookies Contain Undeclared Allergen. Two cookie varieties from Tate's Bake Shop of Southampton, New York—Tate's 7 oz. Chocolate Chip Cookies and Tate's 7 oz. Gluten Free Ginger Zinger Cookies—have been recalled because these cookies may contain undeclared walnuts, an allergen. The Food and Drug Administration … [Read more...] about Two Cookie Varieties from Tate’s Bake Shop Recalled for Undeclared Walnuts
Potassium-Lowering Medication May Reduce Effectiveness of Other Medications
FDA Conduct A Study Of Potassium-Lowering Medication. Concordia Pharmaceuticals has been directed by the Food and Drug Administration (FDA) to conduct studies of the potassium-lowering drug Kayexalate, because of the drug interactions that may reduce the effectiveness of other medications. Current label information for … [Read more...] about Potassium-Lowering Medication May Reduce Effectiveness of Other Medications
GoGo squeeZ Children’s Snack Food Company Recalls Applesauce Products Due to Mold
GoGo Squeez Recall Applesauce Products. GoGo squeeZ, which produces fruit and vegetable snack foods for children in squeezable pouches, has announced the voluntary recall of specific pouches and cartons of applesauce that may be contaminated by mold. The company published a letter to customers on its web site, explaining … [Read more...] about GoGo squeeZ Children’s Snack Food Company Recalls Applesauce Products Due to Mold
Study Finds Rise in Prescription Opioid Misuse and Death
Opioid Abuse Of Prescription. A study published in the Journal of the American Medical Association suggests that the abuse of prescription opioids increasing. Although researchers found that non-medical use decreased between 2003 and 2013, use disorders and overdose deaths increased. The study was led by Dr. Beth Han of the … [Read more...] about Study Finds Rise in Prescription Opioid Misuse and Death
Eli Lilly Abandons Development of New Cholesterol Drug after Poor Performance in Phase 3 Trial
A Cholesterol Drug Fail To Perform Well. On Monday, drug maker Eli Lilly announced that it was ceasing work on a new cholesterol-lowering drug, after the drug failed to perform well in a phase 3 clinical trial. The drug, evacetrapib, was designed to prevent heart attacks and other cardiovascular problems by modifying … [Read more...] about Eli Lilly Abandons Development of New Cholesterol Drug after Poor Performance in Phase 3 Trial
FDA Class 1 Recall for MicroPort Hip Replacement Device
Serious Hip Replacement Device Recall. The Food and Drug Administration (FDA) has assigned its most serious device recall designation to the recall of China's MicroPort replacement hip joint. The MicroPort Orthopedics' Profemur Long Cobalt Chrome 8 Degree Varus/Valgus Modular Neck device is under Class 1 recall because … [Read more...] about FDA Class 1 Recall for MicroPort Hip Replacement Device
NHTSA Says Fiat Chrysler Under-reported Deaths and Injuries
Fiat Chrysler Obliged To Reveal To Regulators. The National Highway Traffic Safety Administration (NHTSA) said automaker Fiat Chrysler under-reported a "significant" number of deaths, injuries and legal claims that it was obliged to reveal to regulators. NHTSA announced the underreporting after Fiat Chrysler said it had discovered … [Read more...] about NHTSA Says Fiat Chrysler Under-reported Deaths and Injuries
FDA Issues Warning about Neurosurgery Device that May Cause Injuries
Neurosurgery Device Litigation. In the Supreme Court of the State of Nevada, jurors continue to hear arguments in a case over Actos bladder cancer claims. Judge Jerry Wiese is presiding over the case, and told jurors at the beginning of the trial that Takeda purposely destroyed documents related to Actos litigation. He … [Read more...] about FDA Issues Warning about Neurosurgery Device that May Cause Injuries
Researchers Say FDA Should be Cautious in Using
FDA Should Be Cautious About Drugs. Researchers argue that the U.S. Food and Drug Administration should avoid using words like "breakthrough" and "promising" when making announcements about new drugs. The researchers contend that the public may not understand the FDA's particular usage. In ordinary use, "breakthrough" denotes an … [Read more...] about Researchers Say FDA Should be Cautious in Using
Increased Risk of Atypical Hip Fractures Associated with Bisphosphonate Use
Risk Of Hip Fractures With Bisphosphonate. Women with osteoporosis who take bisphosphonate drugs to prevent fractures have an increased risk of atypical hip fractures, new research finds. Javier Gorricho-Mendívil conducted the research for his PhD thesis at the NUP/UPNA-Public University of Navarre (Spain), MedicalXpress … [Read more...] about Increased Risk of Atypical Hip Fractures Associated with Bisphosphonate Use
Ayurvedic Dietary Supplements Recalled Because Of Dangerous Levels Of Lead And Mercury
Ayurvedic Dietary Supplements Are Being Recalled. Eleven Ayurvedic dietary supplements have been recalled because they were found to contain elevated lead and mercury levels. The elevated lead and mercury levels in the Baidyanath brand supplements imported by Butala Emporium of Jackson Heights, New York, may cause health problems, … [Read more...] about Ayurvedic Dietary Supplements Recalled Because Of Dangerous Levels Of Lead And Mercury
Recaro Recalls Two Car Seat Models; Top Tether Can Break Free During Crash
Recaro Recalls Car Seats. Recaro Child Safety is recalling nearly 200,000 car seats over safety concerns, the company is reporting. The recall includes the ProRide and Performance Ride car seats made before June 9, 2015. A part that helps keep the top of the child seat secure could break during a crash, allowing the top of the … [Read more...] about Recaro Recalls Two Car Seat Models; Top Tether Can Break Free During Crash
GM Reaches Settlement in Faulty Ignition Switch Probe
Southern District Announced GM Agreed To Settle Ignition Switch Probe. On Thursday, Preet Bharara, U.S. attorney for the Southern District of New York announced that General Motors had agreed to a $900 million criminal settlement, ending the government's investigation into faulty ignition switches in the Chevy Cobalt, … [Read more...] about GM Reaches Settlement in Faulty Ignition Switch Probe
FDA Updates Clozapine Requirements for Neutropenia Risk
Safety Requirements For Clozapine. The U.S. Food and Drug Administration (FDA) is changing certain safety requirements for ‘Clozapine’, a medication used to treat patients with schizophrenia. According to a Drug Safety Communication issued on Sept. 15, the agency is modifying requirements for monitoring, prescribing, … [Read more...] about FDA Updates Clozapine Requirements for Neutropenia Risk
Patients Taking Invokana and Invokamet Face Increased Risk
patients taking Invokana and Invokamet face increased bone fracture risk Fracture Risk Associated With Invokana and Invokamet. Diabetes patients taking the drugs Invokana and Invokamet (canagliflozin) face increased bone fracture risk, the Food and Drug Administration (FDA) warned in a recent safety communication issued last … [Read more...] about Patients Taking Invokana and Invokamet Face Increased Risk
FDA Warns Of Severe Joint Pain With Diabetes Drugs
Severe Joint Pain with Diabetes Drugs. The U.S. Food and Drug Administration (FDA) has warned that diabetes drugs including Januvia, Onglyza, Tradjenta and Nesina may cause severe and disabling joint pain. In a statement that uses the generic names of the drugs, the agency says “The U.S. Food and Drug Administration (FDA) is warning … [Read more...] about FDA Warns Of Severe Joint Pain With Diabetes Drugs
FDA Investigates Risks of Using Codeine Cough-and-Cold Medicines in Children
Risk Of Using Cough-and-Cold Medicines In Children. The U.S. Food and Drug Administration (FDA) has issued a Drug Safety Communication stating that it is investigating the risks of using cough-and-cold medicines containing codeine in children. The agency said there may be "the potential for serious side effects, including … [Read more...] about FDA Investigates Risks of Using Codeine Cough-and-Cold Medicines in Children
New Zealand to Overhaul Medical Device Regulatory System
Medical Device Regulatory System Significant Defects. About half of the metal-on-metal (MoM) hip implants received by thousands of New Zealanders about a decade ago had significant defects, according to the New Zealand Herald. The Herald says there is no official record of the injuries suffered by people who received the faulty … [Read more...] about New Zealand to Overhaul Medical Device Regulatory System
48 States & Dist. of Columbia Reach Settlement with Amgen
Amgen Agreed To Pay. In a settlement announced last week, Amgen Inc. has agreed to pay $71 million to 48 states and the District of Columbia to settle allegations that the drug maker unlawfully marketed the anemia drug Aranesp and the plaque psoriasis drug Enbrel for unapproved uses. The drug maker, based in Thousand Oaks, … [Read more...] about 48 States & Dist. of Columbia Reach Settlement with Amgen
Deadly Superbug Outbreaks Result in FDA Warning Letters for Duodenoscope Manufacturers
Warning Letters For Duodenoscope. A series of superbug outbreaks in hospitals across the country has resulted in FDA warning letters to Olympus Medical Systems, Pentax Medical, and Fujifilm from the Food and Drug Administration (FDA). In the letters, the FDA cited failure to report infections in a timely manner and problems with … [Read more...] about Deadly Superbug Outbreaks Result in FDA Warning Letters for Duodenoscope Manufacturers
Members of Congress Call for Government Accountability
Congress Call For Government Accountability. Twelve members of Congress have written to the Government Accountability Office (GAO) to ask the agency to investigate why a surgical tool used in gynecologic surgery was sold for two decades before the Food and Drug Administration (FDA) issued safety warnings about the device's … [Read more...] about Members of Congress Call for Government Accountability
Multimillion-Dollar Settlement Resolve Blood-Clot Claims Over Bayer’s Yaz and Yasmin Birth Control Pills
Birth Control Pills Can Cause Strokes And Heart Attack. A settlement reported to total nearly $57 million would resolve allegations that Bayer Corp.'s birth control pills Yaz, Yasmin and Ocella cause strokes and heart attacks. The settlement fund would settle claims pending in a multidistrict litigation in Illinois … [Read more...] about Multimillion-Dollar Settlement Resolve Blood-Clot Claims Over Bayer’s Yaz and Yasmin Birth Control Pills
Recently Approved Medtronic Heart Valve Device under Class 1 Recall
Heart Valve Device Under Class 1 Recall. A component Medtronic's CoreValve Evolut R heart valve device is under Class 1 recall less than two months after receiving Food and Drug Administration (FDA) approval. The recall of the EnVeo R loading system has been designated a Class 1 recall, which is the FDA's most serious … [Read more...] about Recently Approved Medtronic Heart Valve Device under Class 1 Recall
Label on Family of Antibiotics May Not List All the Side Effects
Antibiotics Are Linked To Reports Of Deaths. Fluoroquinolones are a family of antibiotics that include drugs such as Levaquin and Cipro. venture According to ABC Action News, a search of the U.S. Food and Drug Administration (FDA) database shows that Levaquin, Cipro and other similar drugs are linked to 3,000 reports of … [Read more...] about Label on Family of Antibiotics May Not List All the Side Effects
Lawsuit Alleges Surgical Warming Blanket Introduced Infection During Surgery
Lawsuit Against The Manufacturer Of Surgical Warming Blanket. A lawsuit has been filed against Arizant, a wholly owned subsidiary of 3M, manufacturer of the Bair Hugger forced-air surgical warming blanket. The complaint alleges that the plaintiff suffered serious injuries when the Bair Hugger introduced dangerous … [Read more...] about Lawsuit Alleges Surgical Warming Blanket Introduced Infection During Surgery
UPPAbaby Strollers and Seats Recalled Due to Choking Hazard
UPPAbaby Strollers Are Being Recalled. Approximately 79,000 UPPAbaby 2015 CRUZ, 2015 VISTA strollers and 2015 RumbleSeats are being recalled in the United States and Canada due to a potential choking hazard. The bumper bar, which has a foam covering, can present a choking hazard if the child bites it and removes a piece of foam. … [Read more...] about UPPAbaby Strollers and Seats Recalled Due to Choking Hazard
FDA Puts Stronger Heart Attack Stroke Warning on Non-Aspirin NSAIDs
Risk Of Heart Attack And Stroke With Non-Aspirin NSAIDs. Following a review of new safety information, the U.S. Food and Drug Administration (FDA) has placed stronger warnings about the risk of heart attack and stroke on the labels of non-aspirin nonsteroidal anti-inflammatory drugs (NSAIDs). NSAIDs are pain relievers that are … [Read more...] about FDA Puts Stronger Heart Attack Stroke Warning on Non-Aspirin NSAIDs
Adverse Events Spur FDA Reconsideration of Essure Birth Control
Negative Side Effects Move the FDA Toward Reevaluation of Essure Birth Control Device.The U.S. Food and Drug Administration ("FDA") is Reevaluating Essure. Essure is the only Nonsurgical permanent birth control device currently approved by the FDA. How Does Essure Work? In an office procedure, a health care professional inserts a … [Read more...] about Adverse Events Spur FDA Reconsideration of Essure Birth Control
Systemic Cobalt Poisoning Increasingly Recognized with MoM Hip Implants
Cobalt Poisoning From Arthroplasty. A review published in the Journal of Patient Safety evaluates systemic arthroprosthetic cobaltism, or systemic cobalt poisoning from arthroplasty implants, related to corrosion of chrome-cobalt hip implants. The researchers sought to identify all cases of systemic arthroprosthetic … [Read more...] about Systemic Cobalt Poisoning Increasingly Recognized with MoM Hip Implants
New Study Suggests Increased Risk of Birth Defects with Prozac, Paxil
Prozac, Paxil Risk Of Birth Defects. A new study published in the British Medical Journal (BMJ) adds to a body of research suggesting that the use of some antidepressants may be associated with a higher risk of birth defects. Researchers at the Centers for Disease Control and Prevention identified an increased risk of … [Read more...] about New Study Suggests Increased Risk of Birth Defects with Prozac, Paxil
FDA: NSAIDs Increase Risk of Stroke
NSAIDs Risk Of Heart Attack Or Stroke. The warning label on non-aspirin, nonsteroidal, anti-inflammatory drugs (NSAIDs) is being revised to reflect an increased risk of heart attack or stroke. In a Safety Alert issued July 9, 2015, the U.S. Food and Drug Administration (FDA) announced that the warning will be strengthened … [Read more...] about FDA: NSAIDs Increase Risk of Stroke
Recall of Covidien Infant and Child Tracheostomy Tubes Because of Breathing Difficulties
Covidien Tracheostomy Tubes Are Being Recalled. On May 8, 2015 Medtronic began notifying hospitals and distributors that lots of its Covidien Shiley tracheostomy tubes for infants and children manufactured after November 29, 2012 were formed with a wider-angle bend than standard models. Medtronic has recalled 70,000 … [Read more...] about Recall of Covidien Infant and Child Tracheostomy Tubes Because of Breathing Difficulties
Baxter Says Peripheral Vascular Patch Recall was Due to Packaging
Baxter Recall Peripheral Vascular Patch. Baxter International, Inc. says new packaging is to blame for the Class I recall of its peripheral vascular patches, Qmed reports. Class I recalls are the most serious type of recall; they are reserved for recalls in which exposure to the drug can reasonably lead to serious health … [Read more...] about Baxter Says Peripheral Vascular Patch Recall was Due to Packaging
Potential Link between Zoloft and Birth Defects Identified in Pfizer Report
Zoloft Linked To Birth Defects. A Pfizer report warning that Zoloft may be linked to birth defects may make it more difficult for the pharmaceutical company to dodge litigation, Bloomberg reports. The April 2014 document shows that Francesca Kolitsopoulous, who was an associate director in Pfizer's Worldwide Safety Strategy unit's … [Read more...] about Potential Link between Zoloft and Birth Defects Identified in Pfizer Report
Use of Bone Morphogenetic Proteins Declines in Spinal Surgeries
Bone Morphogenetic Proteins Use Has Declined. In the last 12 years, bone morphogenetic proteins (BMPs) have been used in spinal fusion procedures, but the authors of a study published in Spine say BMP use has declined in response to concerns about safety and complications. After approval by the Food and Drug … [Read more...] about Use of Bone Morphogenetic Proteins Declines in Spinal Surgeries
FDA: Injury Risk if Soft Tissue Filler Injected into Blood Vessel
Risk Of Injury With Soft Tissue Filler. The Food and Drug Administration (FDA) has issued a safety communication warning of the risk of injury if soft tissue fillers—also known as dermal fillers, wrinkle fillers, or injectable facial implants—are accidentally injected into a blood vessel. The FDA issued the alert to warn health … [Read more...] about FDA: Injury Risk if Soft Tissue Filler Injected into Blood Vessel
Issues with Home Depot Wood Flooring Products May Result in Class Action Lawsuit
Wood Flooring From Home Depot May Result in Class Action Lawsuit. Consumer complaints about wood flooring products from Home Depot's Home Decorators Collection may result in a class action lawsuit. Though these wood laminate products are marketed as easy to install, with a glueless locking system, consumers report that … [Read more...] about Issues with Home Depot Wood Flooring Products May Result in Class Action Lawsuit
Class I Recall Announced for TigerPaw II Heart Device
Class I Recall For TigerPaw II Heart Device. This week, the Food and Drug Administration (FDA) announced the recall of the TigerPaw System II by Maquet Medical Systems. The TigerPaw II is an implantable left atrial appendage (LAA) occlusion device intended for use during heart surgery. The TigerPaw is a surgical staple … [Read more...] about Class I Recall Announced for TigerPaw II Heart Device
Aetna Will No Longer Cover Routine Use of Power Morcellator
Aetna Routine Use Power Morcellator. Aetna Inc. has announced that it will no longer cover routine use of the laparoscopic power morcellator, a surgical tool commonly used in fibroid surgery and hysterectomy. Regulators have determined that the morcellator can spread hidden cancer in women. Aetna is the nation's third largest … [Read more...] about Aetna Will No Longer Cover Routine Use of Power Morcellator
JAMA Report Examines Risks of Using Suturing Device Off-Label
Suturing Device In Patients Could Be Dangerous. A report published online May 4 in JAMA Internal Medicine found that the off-label use of a suturing device in patients with atrial fibrillation could be dangerous, HealthDay News reports. The report focused on the Lariat device, manufactured by SentreHEART. Researchers … [Read more...] about JAMA Report Examines Risks of Using Suturing Device Off-Label
Long-term Data Raises Concerns about Essure Contraceptive Device
Essure Contraceptive Device Cause Serious Injuries. The Essure contraceptive device was considered a breakthrough for women when it came on the market more than ten years ago: it provided a non-surgical sterilization procedure that could be performed in a doctor's office in about ten minutes and promised a quick recovery. … [Read more...] about Long-term Data Raises Concerns about Essure Contraceptive Device
