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Zimmer Biomet, Inc. recalls Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-200152
Recalled January 25, 2017 · FDA recall Z-1025-2017 · Zimmer Biomet
Hazard
Product complaints indicated that the part and lot numbers on the packaging differed from the physical product inside the packaging. Risk of delay in surgery. · FDA Class II
Units
19
Sold at
USA (nationwide) and Internationally to ARGENTINA
Description
Product complaints indicated that the part and lot numbers on the packaging differed from the physical product inside the packaging. Risk of delay in surgery.
Product
Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-200152
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →