Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required Recalled by Zimmer Spine, Inc. Due to Zimmer Biomet is initiating a Medical Device Correction...
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 Spine, Inc. directly.
Affected Products
Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required for solid bone fusion and helps reduce spinal deformities and fractures.
Quantity: 3484
Why Was This Recalled?
Zimmer Biomet is initiating a Medical Device Correction Notice to provide updated cleaning and disinfecting instructions for use of the Instinct¿ Java¿ System (IFU reference: 046WAN0000T) and Universal Clamp¿ System (IFU reference: SNA027-N-90001).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Spine, Inc.
Zimmer Spine, Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report