Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right Recalled by Orthosensor, Inc. Due to Some sensors were reported to have fluid inside...
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 Orthosensor, Inc. directly.
Affected Products
OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right, REF ZBH-PSNCRGH712-R.
Quantity: 68 devices
Why Was This Recalled?
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Where Was This Sold?
This product was distributed to 7 states: CA, FL, IL, IN, MI, NY, NC
About Orthosensor, Inc.
Orthosensor, Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report