Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ROSA Surgical Device 2.5.8 Recalled by Zimmer Biomet, Inc. Due to Potential failure of a force feedback sensor that...
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
ROSA Surgical Device 2.5.8, a computer-controlled electromechanical arm to guide standard neurosurgical instruments.
Quantity: 31 units
Why Was This Recalled?
Potential failure of a force feedback sensor that may result in continued movement of an operating arm (rather than an immediate stop as intended).
Where Was This Sold?
This product was distributed to 5 states: AR, GA, MI, OH, TX
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