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Zimmer Biomet, Inc. recalls Ultra-Drive Hose/Drape Assembly, Reference Number 423833 - Product Usage: Item used with the UltraDrive System to provid
Recalled July 24, 2019 · FDA recall Z-1962-2019 · Zimmer Biomet
Hazard
The products do not have sufficient data to support the labeled shelf life of 10 years. · FDA Class II
Units
8478 total
Sold at
Worldwide distribution - US nationwide distribution and countries of Australia, Brazil, Canada, Chile, China, Columbia, Hong Kong, India, Japan, Malaysia, Netherlands, and Taiwan.
Description
The products do not have sufficient data to support the labeled shelf life of 10 years.
Product
Ultra-Drive Hose/Drape Assembly, Reference Number 423833 - Product Usage: Item used with the UltraDrive System to provide proper irrigation during the cutting and removal of bone and acrylic bone cement in orthopedic applications.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →