Recall

Reckitt Recalls Nutramigen Infant Formula for Bacterial Contamination

January 4, 2024 - Closing out the year, Reckitt, which owns Mead Johnson Nutrition (MJN), voluntarily recalled six batches of Nutramigen Powder, an infant formula sold under the Enfamil brand, on December 31, 2023. The company reported that a risk of contamination with Cronobacter sakazakii prompted the recalls. This recall rounds out a year-long cycle of infant...


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FDA Issues Update on the Philips BiPAP and CPAP Recalls

by Veronica Salib

Last week, the United States Food and Drug Administration released a statement updating consumers and industry leaders on the Philips Respironics recalls due to the potential risks associated with...

FDA Recalls Several J&J Medical Devices After Reports of Burn Injuries

by Hayden Schmidt

Tuesday, the FDA issued a Class I recall of reusable patient return electrodes produced by Johnson and Johnson subsidiary Megadyne Medical Products after receiving reports of patients suffering burn...

FDA Issues Warning on Raw Oysters Contaminated with Norovirus

by Veronica Salib

On June 16, 2023, the FDA issued a statement warning restaurants, retailers, and consumers to avoid serving, selling, or consuming raw oysters from Dai One Food Co, Ltd, and Central Fisheries Co, Ltd,...

FDA Identifies Class I Recall on Philips CPAP and BiPAP Machines

by Veronica Salib

On April 7, 2023, the FDA identified a Class I recall on the Philips Respironics CPAP and BiPAP machines due to inaccurate or insufficient therapy. The devices, intended for treating sleep apnea, had a...

ECRI Highlights Communication Gaps in Medical Device Recalls

by Veronica Salib

In a recent news release, the Emergency Care Research Institute (ECRI) highlighted gaps in communication regarding medical device recalls, noting that these gaps could be a significant threat to...

FDA Announces Malfunctions in Abbott’s MitraClip Device

by Veronica Salib

Mitral regurgitation typically requires a heart valve repair or replacement. Abbott’s MitraClip Clip Delivery System was approved by the FDA in 2013 as a heart valve repair device. However, on...

FDA Recalls Philips BiPAP and CPAP Machine Masks

by Veronica Salib

On September 6, 2022, the FDA shared that Philips recalled specific Philips Respironics masks for BiPAP and CPAP machines. The FDA’s news release shares that these devices have magnets in them,...

Hepatitis A Outbreak Linked to Organic Strawberries Sold in the US and Canada

by Alivia Kaylor

The FDA, CDC, and state and local partners have been investigating a recent hepatitis A outbreak potentially linked to fresh organic strawberries in the United States and Canada. Epidemiologic and...