Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Recalled by Zimmer Biomet, Inc. Due to Potential issue associated with the instrument -end of...
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
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
Quantity: 67 units
Why Was This Recalled?
Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach
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