Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zimmer Dermatone AN Recalled by Zimmer Surgical Inc Due to Devices may have a loose control bar, which...
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 Surgical Inc directly.
Affected Products
Zimmer Dermatone AN, Model No. 88710100
Quantity: 140
Why Was This Recalled?
Devices may have a loose control bar, which could compromise the ability to control the thickness of the graft. Devices could also have a loose width plate that if undetected, could result in an imperfect, yet still usable graft. Potential risks include harvesting a skin graft of a thickness much greater than intended, described as patient gouged, minor delay of surgery, and sub-optimal (but usable) graft.
Where Was This Sold?
This product was distributed to 17 states: AL, AZ, CA, FL, IL, IA, MA, MI, MN, MS, NH, NJ, NY, OH, RI, SD, TX
About Zimmer Surgical Inc
Zimmer Surgical Inc has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report