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      J&J Settles Talc Mesothelioma Settlement

      By Sandra Dalton, Staff Writer On January 6, 2020, Superior Court Judge Stephen Kaus announced that Johnson & Johnsons (J&J) had agreed to … [Read More...]

      Fuentes Farms, LLC Recalls Product Because of Possible Health Risk

      Summary Company Announcement Date: June 13, 2025 FDA Publish Date: June … [Read More...]

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Women with Essure 10 Times as Likely to Require Surgery

October 15, 2015 By US Recall News Leave a Comment

A new study found that women implanted with the contraceptive device Essure were 10 times as likely to require additional surgery within one year as those who had chosen tubal ligation. This only adds to concerns about the device. The U.S. Food and Drug Administration (FDA) received 2,259 complaints about Essure in 2014 and another 1,363 in the … [Read more...]

Filed Under: Essure, Featured, Medical Devices Tagged With: Essure

The Mounting Case against Xarelto from FDA Direct Adverse Drug Reports

October 12, 2015 By US Recall News Leave a Comment

In just the last four years, the FDA has raised many separate clarifications with Johnson & Johnson about the blood thinning drug Xarelto. These have included extra black box warnings about the possible contraindications, additional advertising requirements and further possible side effects that were not included on the original FDA approval in … [Read more...]

Filed Under: Featured, Xarelto Tagged With: Xarelto

Hip Replacement Surgery and the Bair Hugger Device

October 9, 2015 By US Recall News Leave a Comment

It is common practice to use a warming device, such as 3M’s Bair Hugger, during hip and knee replacement surgeries. This is to guard against the risk of hypothermia and to ensure normal blood flow during the operation. The Bair Hugger has been in common use for over 25 years, and 3M claims that almost 180 million operations have been carried out … [Read more...]

Filed Under: Bair Hugger, Featured Tagged With: Bair Hugger

The False Marketing of Risperdal

October 8, 2015 By US Recall News Leave a Comment

Risperdal has been licensed by the FDA since February 1994 for use in psychotic episodes, with a particular emphasis on schizophrenia. It is made by Johnson & Johnson, who most of us know from their range of consumer products, such as baby powder and Listerine mouthwash. However, what is less well known is that Johnson & Johnson make most … [Read more...]

Filed Under: Featured, Risperdal Tagged With: Risperdal

J&J Spends Hundreds of Millions to Promote Xarelto, The Blood Thinner that Kills

October 7, 2015 By US Recall News Leave a Comment

The blood thinner market in the United States was worth over $8 billion in 2012 and is expected to grow to over $15 billion by 2018, according to a June 2013 report by pharmaceutical analysts EvaluatePharma. Xarelto, one of a new type of anti-coagulants that doesn't require individual dosing (unlike category leader Warfarin) is big business for … [Read more...]

Filed Under: Featured, Xarelto Tagged With: Xarelto

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Economic Consulting

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Fuentes Farms, LLC Recalls Product Because of Possible Health Risk

June 13, 2025 By The FDA

Turkana Food Inc. Recall Flora Dried Apricots with Undeclared Sulfites on Product Labeling Because of Possible Health Risk

June 12, 2025 By The FDA

Vita-Warehouse Corp. Issues Allergy Alert on Undeclared Peanut Allergen in ALDI Welby®, Berkley Jensen®, and VitaGlobe™ Vitamin B12 Gummy Products

June 12, 2025 By The FDA

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

More than One Million Anker Power Banks Recalled Due to Fire and Burn Hazards; Manufactured by Anker Innovations

June 11, 2025 By The CPSC

Mammut Sports Group Recalls Skywalker Pro Via Ferrata Sets Due to Risk of Serious Injury or Death from Fall Hazard

June 11, 2025 By The CPSC

Endless Pools Recalls Manual Retractable Pool Covers Due to Drowning and Entrapment Hazards; Risk of Serious Injury and Death

June 11, 2025 By The CPSC

TTI Outdoor Power Equipment Recalls RYOBI 40-Volt 24-Inch Cordless Hedge Trimmers Due to Laceration Hazard

June 11, 2025 By The CPSC

Medtronic Announces Voluntary Recall of Select Newport™ HT70 and Newport™ HT70 Plus Ventilators and Certain Related Newport™ Service Parts

June 11, 2025 By The FDA

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

TTI Outdoor Power Equipment Recalls RYOBI 40-Volt 24-Inch Cordless Hedge Trimmers Due to Laceration Hazard

June 11, 2025 By The CPSC

Medtronic Announces Voluntary Recall of Select Newport™ HT70 and Newport™ HT70 Plus Ventilators and Certain Related Newport™ Service Parts

June 11, 2025 By The FDA

Hofood99 Inc Recalls Enoki Mushroom Due to Possible Health Risk

June 11, 2025 By The FDA

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Recent Posts

  • Fuentes Farms, LLC Recalls Product Because of Possible Health Risk
  • Turkana Food Inc. Recall Flora Dried Apricots with Undeclared Sulfites on Product Labeling Because of Possible Health Risk
  • Vita-Warehouse Corp. Issues Allergy Alert on Undeclared Peanut Allergen in ALDI Welby®, Berkley Jensen®, and VitaGlobe™ Vitamin B12 Gummy Products
  • Bugaboo North America Recalls Giraffe High Chairs Due to Risk of Serious Injury or Death from Fall Hazard
  • Agro Superior Group Recalls Oliver & Smith Mattresses Due to Risk of Serious Injury or Death from Fire Hazard; Violation of Federal Standard for Mattress Flammability
  • More than One Million Anker Power Banks Recalled Due to Fire and Burn Hazards; Manufactured by Anker Innovations
  • Mammut Sports Group Recalls Skywalker Pro Via Ferrata Sets Due to Risk of Serious Injury or Death from Fall Hazard
  • Endless Pools Recalls Manual Retractable Pool Covers Due to Drowning and Entrapment Hazards; Risk of Serious Injury and Death
  • TTI Outdoor Power Equipment Recalls RYOBI 40-Volt 24-Inch Cordless Hedge Trimmers Due to Laceration Hazard
-- See More Recall News

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