Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ultra-Drive Hose/Drape Assembly Recalled by Zimmer Biomet, Inc. Due to The products do not have sufficient data to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Biomet, Inc. directly.
Affected Products
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.
Quantity: 8478 total
Why Was This Recalled?
The products do not have sufficient data to support the labeled shelf life of 10 years.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report