Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 421–440 of 1,000 recalls
Medline Industries, LP
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Medline Industries, LP
Unapproved design changes to the products outside of the 510(k) clearance.