Stryker Leibinger GmbH & Co. KG: Medical Device Recall in 2023 - (Recall #: Z-1234-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis

Product Classification:

Class II

Date Initiated: December 6, 2022

Date Posted: March 15, 2023

Recall Number: Z-1234-2023

Event ID: 91479

Reason for Recall:

Device was shipped without having regulatory approval.

Status: Ongoing

Product Quantity: 1 unit

Code Information:

TMJ Reconstruction Prosthesis, Catalog #2208151054, Lot Number W67725 UDI/DI: B004YYMMDDNNNNLM0

Distribution Pattern:

Distribution of one unit only to a single customer in MA (USA)

Voluntary or Mandated:

Voluntary: Firm initiated