News

Hosted on MSN9mon
The FDA calls them "recalls," yet the targeted medical devices often remain in use
With medical devices, recalls are not always what they seem. In some recalls, including some of the most serious, the FDA and the manufacturers let doctors and hospitals continue to use the devices.
Consumer Reports13y
Dangerous medical implants and devices
Tens of millions of Americans live with medical devices ... analysis of the FDA's database of adverse events. Implanted in more than a half-million Americans with serious heart disorders, the ...
USA Today1mon
FDA Classifies Q’Apel Medical Inc.’s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I
What to know. ‘Yellowstone’ baked beans inspired by TV show recalled by FDA for undeclared allergen Volvo recalls more than 400,000 cars for rearview camera issue: See impacted models Tomatoes ...
Medical Xpress21d
Experts report urgent need for pediatric heart support devices
Patients awaiting a heart transplant are often implanted with ... for pediatric heart devices. The network is working with the U.S. Food and Drug Administration (FDA) to expand the use and monitor ...
WHIO29d
FDA Classifies Q’Apel Medical Inc.’s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I
On April 7, 2025, the U.S. Food and Drug Administration (“FDA” or “the agency”), classified Q’Apel Medical, Inc.’s (“Q’Apel” or “the company”) voluntary recall of 1,617 units ...