Tag Archives: Drug Recall

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Medtronic Infuse Studies Faulted for Downplaying Side Effects

Medtronic Inc.’s published studies for its Infuse bone graft product may have downplayed serious side effects, according to an analysis published last year in The Spine Journal. The study, which drew on U.S. Food & Drug Administration (FDA) documents and other data sources, suggests that up to half of ...

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Smokers More Vulnerable to Joint Replacement Failures

People who smoke cigarettes before and after receiving a total joint replacement, such as a hip replacement device or knee implant, are far more likely to endure revision surgeries on those implants than people who don’t smoke.

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MTA Bus Crash and Two Cars Injures 23 at Utica Ave. & Clarendon Rd

Crash Involving MTA Bus and Two Cars Injures 23

Police are investigating an accident in Brooklyn on Wednesday afternoon that injured 23 people, 3 of them critically, when a car was knocked into the path of an MTA bus.

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Medtronic Infuse Lawsuit Alleges Off-Label Use Cause Painful Complications

A man in Louisiana has filed suit against Medtronic Inc. over injuries allegedly cause by off-label use of its Infuse Bone Graft product. The plaintiff, who received Infuse during transforaminal spinal lumbar fusion surgery, claims that the bone growth protein caused unwanted bone growth along his spine, worsening the back ...

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1,000+ Australians Join DePuy ASR Hip Implant Class Action Lawsuit

A class action lawsuit filed in Australia over DePuy Orthopaedics’ recalled metal-on-metal ASR Hip Implants has signed up more than 1,000 plaintiffs. The attorneys representing the Australian ASR Hip Implant lawsuit plaintiffs recently told The Courier-Mail that damages in the lawsuit are expected to be worth more than $200 million. One ...

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Johnson & Johnson’s Ethicon Division to End Sales of Gynecare Prolift, Three Other Transvaginal Mesh Devices

Johnson & Johnson’s Ethicon Inc. division revealed yesterday that it will end sales of its Gynecare Prolift device and three other transvaginal mesh products. The plan to stop selling the four products was set forth in a letter filed by the company in the Ethicon transvaginal mesh multidistrict litigation ...

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Estate of Kentucky Man Alleges Wrongful Death Due to Actos Bladder Cancer

National law firm, Parker Waichman LLP, just filed a lawsuit on behalf of the estate of a Kentucky man who developed bladder cancer and subsequently died, allegedly due to the use of diabetes drug, Actos. The lawsuit names Takeda Pharmaceuticals America, Inc., Takeda Pharmaceuticals USA, Inc., Takeda Pharmaceuticals North America, ...

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Actos Bladder Cancer Lawsuits Continue, New Complaint Filed by Tennessee Resident

Actos bladder cancer lawsuits continue, with a new complaint filed by a resident of Tennessee. The national law firm, Parker Waichman LLP, represents the Tennessee man who alleges that Actos caused his bladder cancer.

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Medtronic Plans Layoffs, as Infuse Bone Graft Controversy Continues to Weigh on Spinal Business

Medtronic’s spinal division continues to take a huge hit thanks to the controversy surrounding its Infuse Bone Graft product. According to a report from MassDevice.com, the company’s latest earnings report stated that the division saw Infuse sales decline 26% in the first quarter of 2012, and now Medtronic is talking ...

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Conspiracy Claims in Talcum Powder Case Survive Motion to Dismiss

Conspiracy Claims in Talcum Powder Case Survive Motion to Dismiss

E. District of Missouri denied motion to dismiss conspiracy claims. Lawsuit alleges the defendants conspired to misrepresent true dangers with use of talcum powder.

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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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