Tag Archives: product recall

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FDA Questions Device Makers about Duodenoscope Cleaning Procedures

Following Deadly Outbreaks, FDA Questions Device Makers about Duodenoscope Cleaning Procedures

In light of a recent outbreak linked to contaminated duodenoscopes, the U.S. Food and Drug Administration (FDA) is questioning manufacturers about their methods for cleaning the devices, the New York Times reports. The specialized scopes, which have been linked to several outbreaks in recent years, most recently infected seven patients ...

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Metal-on-Metal Hip Replacement Concerns Grow in Canada

Canadian patients and doctors are voicing more concerns about metal-on-metal hip replacements, as health regulators around the world continue to investigate the safety of the devices. According to a report from the CBC, four companies have recently either recalled or suspended sales of metal-on-metal hip replacement devices, while a number ...

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Pradaxa Named in Most FDA Adverse Event Reports for Deaths, Hemorrhage, Kidney Failure and Stroke

The controversial blood thinner, Pradaxa, surpassed all other drugs monitored by the U.S. Food & Drug Administration (FDA) in adverse event reports made to the agency last year. According to the Institute for Safe Medicine Practices’ (ISMP) latest QuarterWatch report, Pradaxa also topped the list for reports of deaths, ...

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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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Exposure to Common Pesticide May Increase ADHD Risk

Exposure to Common Pesticide May Increase ADHD Risk

A new study has found that exposure to a common household pesticide may increase the risk of attention deficit hyperactivity disorder (ADHD) in children.

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Colorado Woman Sues American Medical Systems Over Transvaginal Mesh Injuries

Parker Waichman LLP, a national law firm, just filed a lawsuit on behalf of a Colorado woman allegedly injured by transvaginal mesh products manufactured by American Medical Systems, Inc. The suit was filed on May 21, 2012 in the U.S. District Court for the Northern District of California (Case No. ...

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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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Actos, Avandia May Up Risk for Diabetic Macular Edema

A West Virginia man fitted with a metal-on-metal version of DePuy Orthopaedics’ Pinnacle Hip Implant System has filed suit against the company and its parent, Johnson & Johnson, alleging the device caused him to suffer pain and elevated cobalt levels. The Plaintiff is being represented by the national law ...

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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 ...

Study Finds SSRI Antidepressant Side Effects Outweigh Their Benefits

A new study is raising more concerns about the safety of commonly used antidepressants, including selective serotonin reuptake (SSRI) inhibitor antidepressants. Investigators who conducted the study, which is published in the journal Frontiers in Psychology, posit that increased knowledge of the negative effects of SSRIs and other antidepressants could reduce ...

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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

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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

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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

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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

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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

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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

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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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