Zimmer Surgical Inc recalls Zimmer Dermatome AN, Model/Catalog Number: 88710100
- Recall date
- November 24, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0925-2026
- FDA classification
- Class II
- Brand / firm
- Zimmer Surgical Inc
- Sold / distributed
- 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…
Why it was recalled
The devices may have a misaligned thickness control bar.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Zimmer Dermatome AN, Model/Catalog Number: 88710100
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