Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ROSA Spine 1.0.2 Stereotaxic instrument Computer-assisted surgical device. Intended for Recalled by Zimmer Biomet, Inc. Due to Robot arm being sent to the wrong position
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 Spine 1.0.2 Stereotaxic instrument Computer-assisted surgical device. Intended for the spatial positioning and orientation of instrument holders to be used by surgeons.
Quantity: 1
Why Was This Recalled?
Robot arm being sent to the wrong position
Where Was This Sold?
This product was distributed to 11 states: CA, FL, IL, KY, MA, MN, NY, NC, OH, PA, DC
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