Reconstruction Prosthesis Correction: Stryker Updates Use Instructions For Patient-fitted Tmj Implants

Stryker is updating instructions for its patient-fitted TMJ (temporomandibular joint) implants because of an error in where the screw hole is positioned on the device. The correction affects both unilateral (single-side) and bilateral (both-side) TMJ implants. Patients who have received these implants may be impacted by this update.

Product

Patient-Fitted TMJ Implants

Reason

Stryker is updating use instructions for TMJ Unilateral and Bilateral Implants due to a discrepancy in the positioning of the screw hole.

Category

medical device recall

Country

United States

Agency

FDA-MEDWATCH-RSS

Recall date

2026-04-15

Status

Ongoing

Official recall notice from FDA-MEDWATCH-RSS

Recall details on Nibble Recalls: https://trynibble.app/recalls/14188e9b-8677-41f9-9415-0883c6c9213d