FDA-Device2025-12-24Class IIPROCESSING DEFECT
Zimmer Dermatome AN surgical device recalled for misaligned thickness control
Check Zimmer Dermatome AN device serial number
Zimmer Surgical Inc. is recalling certain Dermatome AN surgical devices (Model 88710100) because the thickness control bar may be misaligned. This could affect the device's ability to cut skin grafts to the correct thickness during surgery. No injuries have been reported.
- Check if you have a Dermatome AN Model 88710100 with lot numbers 65900465, 65944825, 66016265, or 66121190
- Verify your device's serial number against the FDA recall list
- Contact Zimmer Surgical Inc. for instructions on device replacement or repair
- Do not use the device if it is on the recall list
Hazard
The devices may have a misaligned thickness control bar.
Who it affects
Adults
Illnesses reported
None reported
Sold states
Distribution regions: USA, Hong Kong, Thailand, Japan, Korea, Australia, Taiwan, India, Malaysia, Singapore, China, Canada, EMEA, Mexico, Trinidad & Tobago, Panama, Guatemala Refer to the attached ZFA 2025-00141_Initial Consignee List and ZFA 2025-001141_Initial Distribution History containing the distribution and the identification of the domestic consignees.
Affected count
498 units
Manufactured in
200 W Ohio Ave, Dover, OH, United States
Products
Zimmer Dermatome AN, Model/Catalog Number: 88710100
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0925-2026More Zimmer Biomet recalls
- FDA-Device2026-07-08Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual Hose with CPC Connectors Model/Catalog Number: 60-1812-101-00 Software Version: N/A Product Description: Dual Sterile Extension Hose with PLC Connector Component: N/A
- FDA-Device2026-07-08Zimmer Surgical A.T.S. 4000 TS Tourniquet Hoses recalled for sterility breach risk
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