The FDA Finally Visited an Indian Drug Factory Linked to U.S. Deaths. It Found Problems.
The inspection comes after a ProPublica investigation revealed that drugs made at the Glenmark Pharmaceuticals plant ...
The Healthy @Reader's Digest5d
A Heart Attack & Stroke Medication Has Been Recalled Nationwide
It's reported more than 8 million Americans take a blood thinner. One has been recalled for potential absorption issues.
FDA classifies recall of Medtronic embolization devices as 'most serious'
The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", ...
Daily Voice1d
Benadryl Recall Issued Over Packaging Flaw That Endangers Children, Cpsc Says
A recall has been issued for Benadryl due to a bottle safety flaw that could put children at risk of poisoning, officials ...
American Hospital Association12d
4 Steps to Improve Medical Device Recall Tracking
As of late February, there were 147 medical device recall events and 20 of them, or 13.6%, were Class I, according to a Modern Healthcare report.
Target recall: 200,000 cans of Del Monte vegetables recalled over possible contamination
California-based Del Monte Foods, Inc. has recalled 8,242 cases of its Target brand Good & Gather Cut Green Beans because due ...
Daily Voice on MSN1d
Aldi Recalls Cheese From CT Stores Over Possible Metal Contamination: FDA
The U.S. Food and Drug Administration has issued a recall of a cheese sold at Aldi stores in Connecticut, Michigan, Ohio, and ...
Recall: Green beans sold at Target may be contaminated
(NEXSTAR) — Del Monte Foods is recalling 8,242 cases of its green beans, which were sold at Target stores across multiple ...
WFMJ3d
Recall issued for 4,800 pouches of colby jack cheese sold at ALDI over metal concerns
Great Lakes Cheese Co. Inc. is recalling about 400 cases of Happy Farms by ALDI Colby Jack shredded cheese due to potential ...
Medical Device Network on MSN2d
FDA tags Becton, Dickinson and Company infusion software recall as Class I
Problematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few years.