Home / Recalls / Medical Devices
Zimmer Biomet, Inc. recalls Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
Recalled June 7, 2017 · FDA recall Z-2198-2017 · Zimmer Biomet
Hazard
Durability characteristics of reusable instruments were not established · FDA Class II
Units
Greater than 10,000,000 last 10 years
Sold at
Nationwide Worldwide
Description
Durability characteristics of reusable instruments were not established
Product
Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →