PlainRecalls
FDA Devices Moderate Class II Ongoing

Zimmer Dermatome AN, Model/Catalog Number: 88710100

Reported: December 24, 2025 Initiated: November 24, 2025 #Z-0925-2026

Product Description

Zimmer Dermatome AN, Model/Catalog Number: 88710100

Reason for Recall

The devices may have a misaligned thickness control bar.

Details

Recalling Firm
Zimmer Surgical Inc
Units Affected
498 units
Distribution
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.
Location
Dover, OH

Frequently Asked Questions

What product was recalled?
Zimmer Dermatome AN, Model/Catalog Number: 88710100. Recalled by Zimmer Surgical Inc. Units affected: 498 units.
Why was this product recalled?
The devices may have a misaligned thickness control bar.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 24, 2025. Severity: Moderate. Recall number: Z-0925-2026.