3B Media News16h
SMITHS MEDICAL RECALLS ENDOTRACHEAL TUBES; EIGHT REPORTS OF INJURY
Smiths Medical has issued an Urgent Medical Device Correction to notify affected global customers of a potential issue with ...
American Hospital Association21h
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.
Dexcom receives FDA warning letter for two U.S. manufacturing facilities
Medical device maker Dexcom said it has received a warning letter from the U.S. Food and Drug Administration following ...
Medical Device Network on MSN5d
FDA issues early alert for Baxter’s Spectrum infusion pump
The agency’s notice highlights that Baxter has issued a letter to affected customers, recommending its Sigma Spectrum ...