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Zimmer Biomet, Inc. recalls ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general
Recalled February 5, 2020 · FDA recall Z-0871-2020 · Zimmer Biomet
Hazard
Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach · FDA Class II
Units
67 units
Sold at
US Nationwide and Foreign: countries of Canada, CHINA, NETHERLANDS
Description
Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach
Product
ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgical instrument
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →