FDA Device Intelligence
HomeDevice types › GEJ

Carrier, Ligature

FDA product code GEJ · Class 1 · General, Plastic Surgery

134
Registered devices
9
Adverse events
4
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2017-04-25Cook Inc.reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products
2017-04-25Cook Inc.reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products
2017-04-25Cook Inc.reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products
2006-10-12Conmed CorporationThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.