Waldemar Link GmbH & Co. KG (Mfg Site) recalls L-Shaped Femoral Augment; Item Numbers: (1) 880-320/12 (Sz. 0 - cemented sm), (2) 880-320/22 (Sz. 0 - cemented lg), (3)

Recalled May 7, 2025 · FDA recall Z-1701-2025 · Waldemar Link GmbH & Co. KG (Mfg Site)

Hazard

The device was delivered with a preassembled Femoral Augment screw that was missing its thread. · FDA Class II

Units

441 units

Sold at

US Nationwide distribution in the states of AL, AZ, CA, CO, FL, GA, IN, IL, KS, LA, MD, MO, NV, OH, TX, VA, WI.

Description

The device was delivered with a preassembled Femoral Augment screw that was missing its thread.

Product

L-Shaped Femoral Augment; Item Numbers: (1) 880-320/12 (Sz. 0 - cemented sm), (2) 880-320/22 (Sz. 0 - cemented lg), (3) 880-321/12 (Sz. 1-2 - cemented sm), (4) 880-321/22 (Sz. 1-2 - cemented lg), (5) 880-323/13 (Sz. 3-4 - cemented sm), (6) 880-323/23 (Sz. 3-4 - cemented lg), (7) 880-325/13 (Sz. 5-6 - cemented sm), (8) 880-325/23 (Sz. 5-6 - cemented lg), (9) 880-327/13 (Sz. 7-8 - cemented sm), (10) 880-327/23 (Sz. 7-8 - cemented lg), (11) 880-329/13 (Sz. 9-10 - cemented sm), (12) 880-329/23 (Sz. 9-10 - cemented lg).

Manufacturer(s)

Waldemar Link GmbH & Co. KG (Mfg Site)

Made in

Germany

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →