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Breaking Legal News

Study Indicates Increased Risk of Heart Attack and Blood Clots after Knee or Hip Replacement

Sep 3, 2015
New research from a team based in Boston shows that osteoarthritis patients who have total knee or hip joint replacement surgery (arthroplasty) face...

FDA Warning Letters Issued to Five Producers of Pure Powdered Caffeine

Sep 3, 2015
On September 1, 2015, the Food and Drug Administration (FDA) issued warning letters to five distributors of pure powdered caffeine, "because these...

Covidien, Puritan Bennett 980 Ventilator Recalled, May Not Deliver Enough Oxygen

Sep 3, 2015
A Class I recall has been issued for the Puritan Bennett 980 Ventilator, manufactured by Covidien, because the system may deliver less air than what...

Lawsuit Filed over Death of Patient who Contracted Fatal Superbug, Allegedly Due to Pentax Scope

Sep 3, 2015
A wrongful death lawsuit has been filed in connection with the superbug outbreaks linked to contaminated duodenoscopes. The suit, which was filed on...

Europe Bans 700 Generic Medicines Because of Flawed Clinical Tests But FDA Allows Them to Remain on Market in U.S.

Sep 1, 2015
The U.S. Food and Drug Administration (FDA) has found no systemic issues affecting the safety or efficacy of generic drugs tested at GVK BioSciences,...

FDA Sends Warning Letters to Three Tobacco Companies over Marketing Claims

Aug 31, 2015
The Food and Drug Administration (FDA) has sent warning letters to three tobacco companies for making "additive-free" and/or "natural" claims on...

FDA Warns of Severe Joint Pain with Diabetes Drugs

Aug 31, 2015
The U.S. Food and Drug Administration (FDA) has warned that diabetes drugs including Januvia, Onglyza, Tradjenta and Nesina may cause severe and...

FDA Seeks Food Companies' Cooperation in Genome Sequencing to Identify Sources of Foodborne Illnesses

Aug 31, 2015
The Food and Drug Administration (FDA) is seeking food company cooperation in whole genome sequencing of pathogens, which will permit FDA officials...

FDA Class 2 Recall for 17,000 Stryker Orthopedic Devices Possibly Damaged in Shipping

Aug 28, 2015
The Food and Drug Administration (FDA) has issued an announcement of the recall of 16,992 Stryker Corporation orthopedic implant devices because of...

Information Prompts FDA to Strengthen Heart Attack and Stroke Warnings for Nonsteroidal Anti-inflammatory Drugs

Aug 28, 2015
In response to recent study results, the Food and Drug Administration (FDA) has directed strengthened warning labels for both prescription and...

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