Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to The surface coating applied to the device is...
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¿ Air Dermatome II Width Plate, 1 in., item number 00-8851-201-00 . Width plates is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope. The Zimmer Air Dermatome II is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities.
Quantity: 70 units
Why Was This Recalled?
The surface coating applied to the device is blistering, peeling and discoloring after usage over time
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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