Recall database

Recalls in Indiana

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 73–76 of 76 recalls

Class IIOngoingZ-1038-2025

Zimmer, Inc. recalls NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C

It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.

Zimmer, Inc.INFeb 5, 2025

Class IIOngoingZ-0834-2025

Cook Biotech, Inc. recalls Cook Medical Biodesign Dural Graft

Incorrect version of IFU was used rather than updated version; and incorrect expiration date was used on two of the products.

Cook Biotech, Inc.INJan 22, 2025

Class IIOngoingZ-0833-2025

Cook Biotech, Inc. recalls Cook Medical Biodesign Hiatal Hernia Graft

Incorrect version of IFU was used rather than updated version; and incorrect expiration date was used on two of the products.

Cook Biotech, Inc.INJan 22, 2025

Class IIOngoingZ-0832-2025

Cook Biotech, Inc. recalls Cook Medical Biodesign Otologic Butterfly Graft

Incorrect version of IFU was used rather than updated version; and incorrect expiration date was used on two of the products.

Cook Biotech, Inc.INJan 22, 2025