Tag Archives: Drug Recall

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Post -Tonsillectomy Morphine Life-Threatening in Children

Post -Tonsillectomy Morphine can be Life-Threatening in Children, Study Finds

A new study published in Pediatrics suggests that morphine can result in life-threatening respiratory problems when given to children after a tonsillectomy.

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Actos Side Effects Lawyers Says Whistleblower Revelations Could Boost Bladder Cancer, Heart Failure Lawsuits

An attorney with a prominent personal injury law firm says an Actos whistleblower lawsuit filed earlier this year could strengthen legal claims alleging the type 2 diabetes medication caused some users to develop bladder cancer and heart failure.

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Oklahoma Woman Latest to Head to Court Over Alleged DePuy ASR Hip Implant Injuries

Lawsuits filed by alleged victims of DePuy Orthopaedics’ recalled ASR hip replacement devices continue to pile up in the multidistrict litigation currently underway in U.S. District Court, Northern District of Ohio. Most recently, a woman from Pryor, Oklahoma, filed suit alleging complications caused by a DePuy ASR hip implant ...

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Zadroga Act Cancer Decision Expected This Week

The federal official tasked with determining what ailments should be covered by the federal Zadroga Act is expected to decide by Saturday if certain cancers will be eligible for compensation. The decision is being eagerly awaited by thousands of first responders who believe they developed cancer due to exposure ...

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First DePuy ASR Hip Implant Lawsuits Head to Trial in December, January

The first trials involving lawsuits filed against DePuy Orthopaedics by recipients of its recalled ASR Hip Implants will begin later this year, and early next year. The first is slated to start on December 3, 2012 in state court in Las Vegas, Nevada. A second DePuy ASR hip implant lawsuit ...

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Federal DePuy ASR Hip Implant Trials Likely to Start This Year

It looks as though the first trials in the DePuy ASR hip implant multidistrict litigation could begin sometime later this year. According to a report from Bloomberg News, during a status conference held yesterday in Florida, attorneys for both plaintiffs and the defense told U.S. District Judge David Katz that ...

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Research Study Confirms Fracking Cause of Ohio Earthquakes

Research Study Confirms Fracking as Cause of Ohio Earthquakes

Fracking operation near Poland Township, Ohio, activated a previously unknown fault in the, causing 77 earthquakes with magnitudes ranging from 1.0 to 3.0 in March 2014.

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Actos, Avandia May Up Risk for Diabetic Macular Edema

A newly published study is raising concerns that patients who take Actos or Avandia may face an increased risk of developing diabetic macular edema, an eye disorder that can result in vision loss. The study, published in the Archives of Internal Medicine, found that type 2 diabetics who use thiazolidinediones, ...

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Johnson & Johnson Facing More Metal-on-Metal Hip Implant Woes, as DePuy Pinnacle Complaints Rise

Having already spent around $3 billion on its DePuy Orthopaedics ASR hip implant recall, Johnson & Johnson is facing another potential debacle involving a metal-on-metal version of its Pinnacle Hip Replacement System. According to a report from Reuters, Johnson & Johnson and its DePuy unit already face some 1,600 metal-on-metal ...
DeflateGate’s Effects Impact Legal Gambling & the Economy

DeflateGate’s-Effects-Impact-Legal-Gambling-and-the-Economy

The NFL has initiated a probe into the New England Patriots following allegations that the team intentionally used overly deflated footballs.

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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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