Defective Drug Lawyers
Get Help From a Knowledgeable Defective Drug Lawyer Defective drugs are medications that cause physical or psychological injury. Often, these injuries relate to recalled drugs, drugs that were not adequately tested for all of their potential side effects, manufacturing errors, dosage mistakes, inadequate warnings, or mislabeling. If … [Read more...]
Hospira Recalls Hydromorphone Injection on Overdose Concern
Hospira, Inc. just announced a recall of its Hydromorphone Injection due to overdose concerns, the U.S. Food & Drug Administration (FDA) just announced. The recall involves one lot of Hydromorphone Injection, USP, 2 mg/mL (C-II), 1 mL fill in 2.5 mL Carpuject™, NDC 0409-1312-30, and followed a reported complaint of a single … [Read more...]
Class I Recall Issued For Potentially Contaminated Ultrasound Gel
A Class I recall has been issued for potentially contaminated ultrasound gel, the U.S. Food & Drug Administration (FDA) just announced. A Class I recall involves a situation in which there exists a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or … [Read more...]
Epinephrine Injections Recalled For Discoloration, Particle Contamination
Epinephrine injections, distributed by American Regent, are being recalled for discoloration and particle contamination, the U.S. Food & Drug Administration (FDA) just announced. The nationwide recall is being conducted at the retail/hospital level and involves Epinephrine Injection, USP, 1:1000, 1 mL Ampules 
NDC … [Read more...]
X-Rock Male Supplement Recalled
X-ROCK INDUSTRIES, an independent distributor of X-Rock products, is recalling some of its X-Rock Male Supplements, the U.S. Food & Drug Administration (FDA) announced. The finished product of X-Rock for Men—sold by XROCK INDUSTRIES and under the brand name X-Rock—was tested and found to contain an analogue of an ingredient in … [Read more...]
Hospira Recalls Morphine Injections, Syringes may be Over-Filled
Hospira, Inc. is recalling morphine injections because the syringes may be over-filled, the U.S. Food & Drug Administration just announced. The recall involves one lot of Morphine Sulfate Injection USP, 4 mg/mL (C-II), 1 mL fill in 2.5 mL Carpuject, NDC 0409-1258-30. The action was prompted following a customer report of two … [Read more...]
Warfarin Recall Issued, Tablets may be Mislabled
Upsher-Smith Laboratories, Inc., of Maple Grove, Minnesota is issuing a Drug Recall for one lot—Lot # 284081—of Jantoven® Warfarin Sodium, USP, 3mg Tablets. This is an anticoagulant with an expiration date of September 2012, NDC # 0832-1214-00. Upsher-Smith Laboratories initiated the recall after a single bottle labeled as … [Read more...]
Shaping Beauty Recalls Weight Loss Pills
Shaping Beauty, Inc. of Southampton, Pennsylvania, has been informed by the U.S. Food and Drug Administration (FDA) that a weight-loss dietary supplement it sold and marketed contains an undeclared drug ingredient. FDA lab analyses of the defective drugs distributed by Shaping Beauty were found to contain undeclared Sibutramine … [Read more...]
