Top Reasons Why Products Are Recalled
This article was originally published in The Silver Sheet
Executive Summary
FDA REVEALS THE MOST COMMON ROOT CAUSES for medical device recalls. No. 1: components that do not conform to specifications.
You may also be interested in...
Agency Officials, Experts Offer Advice On Product Recalls
RECALLS WON'T BE AS DIFFICULT if manufacturers handle them properly, FDA says. “Successfully handling recalls is one of the key activities that a firm is going to have to do,” says Kimber Richter, a CDRH medical officer. FDA offers advice on recall notifications and risk evaluations
Second EU MDR Notified Body Designated In France
Four years after the designation of the first notified body in France under the Medical Device Regulation, AFNOR Certification has been named too.