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Zimmer Biomet, Inc. recalls Maximum Variable Pitch Compression Tray Base, Reference Number 231201002 Product Usage: Intended to carry implants a
Recalled January 23, 2019 · FDA recall Z-0734-2019 · Zimmer Biomet
Hazard
There is a potential for silicone shedding during cleaning and sterilization. · FDA Class II
Units
971 i nTotal
Sold at
Worldwide Distribution - US Nationwide, The products were distributed to the following foreign countries: Australia, Chile, Netherlands.
Description
There is a potential for silicone shedding during cleaning and sterilization.
Product
Maximum Variable Pitch Compression Tray Base, Reference Number 231201002 Product Usage: Intended to carry implants and instruments during regular inventory distribution and handling and sterilization in the hospitals
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →