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Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812
Recalled August 21, 2019 · FDA recall Z-2233-2019 · Zimmer Biomet
Hazard
Cleaning processes potentially being ineffective · FDA Class II
Units
23
Sold at
Distributed to the following states in the USA: AZ, CA, DC, GA, IL, KY, LA, MA, MD, MN, NC, NJ, NM, OH,OK, OR, SC, TX. Distributed to Japan and Netherlands.
Description
Cleaning processes potentially being ineffective
Product
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →