Tag Archives: Drug Recall

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Study Links Liquid in E-Cigarette to Viral Infections

Study Links Liquid in Electronic Cigarette to Increased Risk of Viral Infections

The National Jewish Health study, links the liquid used in e-cigarettes to a higher risk of respiratory viral infections, whether the liquid contains nicotine or not.

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Two Men Found Dead of Carbon Monoxide Poisoning

Two Men Found Dead of Carbon Monoxide Poisoning at Long Island, New York Auto Shop

Two men were found dead of apparent carbon monoxide poisoning in a Holbrook, New York, auto-detailing shop Thursday night, Suffolk County police say.

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Government Penalizes 721 Hospitals for High Rates of Infections, Injuries

Medicare is reducing payments to 721 hospitals, one out of every seven hospitals in the nation, for having high rates of “hospital-acquired” conditions (HAC.

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Geodon the antipsychotic drug can Cause Deadly Skin Reaction

Geodon can Cause Deadly Skin Reaction, FDA Warns

The FDA has required a new warning label for the antipsychotic drug Geodon (ziprasidone) to include the risk of a potentially fatal skin reaction.

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Boston Scientific Transvaginal Mesh

Tennessee Woman Alleges Boston Scientific Transvaginal Mesh Product Caused Painful Injuries

More reports of painful injuries are being linked to transvaginal mesh. This time, a Tennessee woman has filed a lawsuit against Boston Scientific over its Advantage Transvaginal Mid-Urethral Sling System.

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Scientist Calls for Federal Regulations for Fracking Pollution

Hydraulic fracturing (fracking) drilling should be governed by federal regulations because its pollution has no awareness of state boundaries.

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Bayer Yaz, Yasmin Blood Clot Lawsuit Settlements Stand at $147 Million

Bayer AG reported yesterday that it continues to settle Yaz and Yasmin birth control pill lawsuits. According to a report from Bloomberg News, the company said in its latest Stockholder Newsletter that it has settled 651 Yaz and Yasmin blood clot lawsuits for a total of $147 million. The average ...

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Lawsuit Alleges Bi-Lateral DePuy ASR Hip Implant Resulted in Elevated Chromium and Cobalt Levels, Need for Revision Surgery

DePuy Orthopaedics and its parent, Johnson & Johnson, continue to be named in lawsuits by metal-on-metal hip replacement recipients who suffered severe injuries, including elevated chromium and cobalt levels, allegedly due to recalled ASR hip implant devices. Most recently, the national law firm of Parker Waichman LLP filed suit on ...

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Whistleblower Wins Retaliation - Canaveral National Seashore

Whistleblower Wins Retaliation Lawsuit

A whistleblower who reported misconduct at Canaveral National Seashore has won a retaliation ruling against the U.S. Department of Interior, Florida Today reports.

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What Action Will the FDA Take on E-cigarettes?

What Action Will the FDA Take on E-cigarettes?

As health and quality concerns trouble the e-cigarette industry, experts and the public await the Food and Drug Administration (FDA)’s action to regulate the devices.

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Class III Voluntary Recall Issued for High Blood Pressure Medication

Class III Recall Issued for High Blood Pressure Medication

As a result of a recent Enforcement Report of the U.S. Food and Drug Administration (FDA), Sun Pharma and Lupin  are recalling over 41.5 thousand drug bottles in the United States. Sun Pharmaceutical Industries Inc. is recalling 12,109 bottles of … Continue reading

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Novartis recalls Agrippal flu vaccine in the U.K. after particles found in vials

Health officials in the U.K. are dealing with a recall on more than 160,000 vials of a flu vaccine just as the season in which they’re most likely to be dispensed hits. According to a report from The Telegraph (U.K.), … Continue reading

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Hydrocodone Bitartrate and Acetaminophen Tablets Recalled for Oversized Tablets

Qualitest Hydrocodone Bitartrate and Acetaminophen Tables are being recalled for oversized tablets, the U.S. Food & Drug Administration (FDA) just announced. Qualitest is a subsidiary of Endo Health Solutions. The nationwide recall involves one lot of Hydrocodone Bitartrate and Acetaminophen … Continue reading

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Nimodipine Capsules Recalled for Crystallization

Nimodipine capsules have been recalled for crystallization issues, the U.S. Food & Drug Administration (FDA) just announced. Sun Pharmaceutical Industries, Inc. is recalling one lot of Nimodipine Capsules, 30 mg, marketed by Caraco Pharmaceutical Laboratories, Ltd. Sun Inc. initiated the … Continue reading

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Bedford Laboratories Recalls Leucovorin Calcium Injection for Contamination

Bedford Laboratories just issued a nationwide recall for its Leucovorin Calcium injection due to contamination, the U.S. Food & Drug Administration (FDA) just announced. The following Leucovorin Calcium Injection,
500mg, lots are involved:

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Hospira Recalls Hydromorphone Injections that may Contain more than Intended Volume

Hospira, Inc. just announced that it s recalling, at the user level, one lot of its Hydromorphone Injection over reported complaints that one of its Carpuject’s contains more than 1 mL label fill volume, the U.S. Food & Drug Administration … Continue reading

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Johnson & Johnson Facilities at Center of Tylenol, Other Drug Recalls Face Greater FDA Scrutiny

A Johnson & Johnson drug plant in Fort Washington, Pennsylvania that made millions of bottles of recalled medicine, including < "http://www.yourlawyer.com/topics/overview/Tylenol-Liver-Damage-Injury-Lawsuit-Lawyer">Tylenol, Benadryl and Motrin, will not be allowed to reopen until the U.S. Food & Drug Administration (FDA) is assured … Continue reading

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FDA Acts against Unapproved Cold, Cough and Allergy Drugs, Orders Hundreds Removed from Market

More than 500 < "http://www.yourlawyer.com/practice_areas/defective_drugs">unapproved prescription cough, cold and allergy medicines – including familiar names like include Lodrane, Cardec, Organidin and Pediahist – have been ordered off the market by the U.S. Food & Drug Administration (FDA). None of the … Continue reading

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Simponi Pens Recalled by Johnson & Johnson for Manufacturing Defect

Johnson & Johnson is recalling < "http://www.yourlawyer.com/practice_areas/defective_drugs">Simponi injection pens in the U.S. and Germany. According to the company, a potential defect could result in an insufficient dose of the rheumatoid arthritis drug, and patients are being advised to use pre-filled … Continue reading

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Avandia Ban Announced in New Zealand

< "http://www.yourlawyer.com/topics/overview/avandia">Avandia is being pulled from the market in yet another country, this time in New Zealand. Sales of the controversial diabetes drug, which has been linked to side effects such as heart attacks and strokes, has been severely restricted … Continue reading

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