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Zimmer Biomet, Inc. recalls The 2nd Assist Knee Positioner
Recalled March 7, 2018 · FDA recall Z-0803-2018 · Zimmer Biomet
Hazard
Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution. · FDA Class II
Units
38,879 units
Sold at
Nationally
Description
Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution.
Product
The 2nd Assist Knee Positioner
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →