Medical Device Network on MSN21h
FDA tags Becton, Dickinson and Company infusion software recall as Class IProblematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few ...
The business, acquired by ICU Medical in 2022, has been dealing with a series of recalls and quality issues over the past ...
The FDA has labeled Smiths Medical's recall of ProPort Implantable Plastic Port as Class I, the most serious kind.
A popular laundry detergent used on delicate clothing has been recalled over a possible bacteria exposure risk. The recall ...
A popular laundry detergent was recently recalled due to bacteria contamination. The bottles were sold on Amazon in January, ...
The Food and Drug Administration has identified a Class I recall of Becton, Dickinson and Company BD Alaris Systems Manager and BD Care Coordination Engine Infusion Adapters due to reports that ...
The Healthy @Reader's Digest on MSN21h
2,300 Bottles of a Trusted Allergy Medicine Were Just Recalled for Federal ViolationData show more than 50 million Americans may combat allergy symptoms, but an agency says an over-the-counter drug's bottle ...
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