Tag Archives: product 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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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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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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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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Decision on Pradaxa Bleeding Lawsuit Multidistrict Litigation Expected Soon

Victims of alleged Pradaxa injuries are awaiting word on whether their lawsuits will be consolidated in a multidistrict litigation. According to a report from The Madison Record, so far just over two dozen Pradaxa bleeding lawsuits have been filed in federal courts throughout the U.S.

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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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Trial over Ethicon Transvaginal Mesh Begins in California

Pelvic mesh devices have become the subject of safety concerns in recent years amidst reports that they can cause serious, sometimes permanent injuries.

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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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Pradaxa not Fit for a Dog, Family of Alleged Pradaxa Bleeding Victim Claims

The family of a Texas woman who died just months before her 60th wedding anniversary believes she would be alive today were it not for Pradaxa (dabigatran). According to a report from the Houston Press, Pradaxa patient Loraine Franklin fell and hit her head last December, resulting in an intracranial ...

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Personal Panic Devices Recalled Due to Malfunction

Personal Panic Devices Recalled Due to Malfunction

Interlogix is recalling 67,000 personal panic devices because they may fail to operate in case of an emergency. According to a recall alert posted on the U.S. Consumer Product Safety Commission (CPSC) website, “The wireless personal panic devices can fail … Continue reading

Posted in Defective Medical Devices | Tagged , , , , |

Medtronic Recalls Thousands of Lots of Various Neurovascular Products

Medtronic Recalls Lots of Various Neurovascular Products

Medtronic PLC just recalled certain lots of four of its neurovascular products. The device maker noted that the recalled devices might lead to a thromboembolic event (blood clot) in patients. The recalled Medtronic neurovascular products are: Pipeline Embolization Device (1742 … Continue reading

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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

Posted in Pharmaceuticals, Product Recalls, Recalled Drugs | Tagged , , , , , , |

Lil’ Luxuries Infant Bath Tubs Recalled due to Risk of Serious Injury

Lil’ Luxuries Infant Bath Tubs Recalled due to Injury Risk

Approximately 86,000 Lil’ Luxuries Infant Bath Tubs with fabric slings have been recalled. The fabric slings on the recalled infant bath tubs may detach from the tub and pose a risk of impact injury or drowning, according to the United … Continue reading

Posted in Defective Products, Health Concerns, Product Recalls | Tagged , , , , |

Evenflo Recalls 3-in-1 Combination Car Seats Due to Safety Risk

Evenflo Recalls Combination Car Seats Due to Safety Risk

A recall is being issued for Evenflo combination car seats due to safety risks. The recall, which affects 30,000 units, was launched following reports that children can loosen the safety harness on their own. If they can loosen the safety … Continue reading

Posted in Defective Products, Product Recalls | Tagged , , , , |

Black Forest Hams Recalled due to Possible Foreign Matter Contamination

Black Forest Hams Recalled due to Possible Contamination

The food company 502 Boundary Blvd. Inc., formerly known as Fletcher’s Fine Foods Ltd., has recalled approximately 8,700 pounds of ham products that may be contaminated with foreign matter, specifically rubber. The U.S. Department of Agriculture’s Food Safety and Inspection … Continue reading

Posted in Defective Products, Food Products, Product Recalls, Recalled Food Products | Tagged , , , , |

Gallo Meats LLC Recalls Sausage, Beef, and Lamb Products

Gallo Meats LLC Recalls Sausage, Beef, and Lamb Products

The United States Department of Agriculture’s (USDA) Food Safety and Inspection Service (FSIS) announced that Gallo Meats LLC of Colville, Washington, recalled Sausage, Beef, and Lamb products because they were produced without benefit of inspection. The recall was subsequently updated … Continue reading

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Potential Listeria Contamination Prompts Blue Bell to Recall Ice Cream

Listeria Contamination Prompts Blue Bell to Recall Ice Cream

A voluntary recall is being issued for Blue Bell Ice Cream produced in its Sylacauga, Alabama facility because there is a chocolate chip cookie dough ingredient supplied by a third party supplier, Aspen Hills, Inc., that may be contaminated with … Continue reading

Posted in Food Poisoning, Food Products, Listeria, Product Recalls | Tagged , , , , , |

Medtronic Recalls Temporary Cardiac Lead Pacing Systems

Medtronic Recalls Temporary Cardiac Lead Pacing Systems

The Food and Drug Administration (FDA) has announced a Class II designation for a recall involving thousands of Medtronic temporary lead pacing systems because there is the potential for them to connect to a hazardous voltage. The recall involves 11,697 of … Continue reading

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Due to Fire Hazard, Nissan Recalls Maxima and Murano Models

Due to Fire Hazard, Nissan Recalls Maxima and Murano Models

Due to a potential fire risk, Nissan is recalling roughly 134,000 2016-2017 Maxima sedans, 2015-2017 Murano crossovers, and 2015-2016 Murano Hybrids. The recall only affects models equipped with Intelligent Cruise Control. According to Auto Blog, the recall is being issued … Continue reading

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