Stryker Leibinger GmbH & Co. KG: Medical Device Recall in 2022 - (Recall #: Z-0715-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032

Product Classification:

Class II

Date Initiated: December 29, 2021

Date Posted: March 9, 2022

Recall Number: Z-0715-2022

Event ID: 89458

Reason for Recall:

Inside the packaging of one reported item a non-conforming product was found. Contrary to the design, the barrier layer was manufactured on the inferior side of the implant versus the superior side.

Status: Terminated

Product Quantity: 74

Code Information:

UDI: 07613252084334; Lot Number: 3R7YHD

Distribution Pattern:

Worldwide distribution - US Nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated