Zimmer Dermatome An, Model/catalog Number: 88710100
Zimmer Dermatome AN Recall Summary Zimmer Surgical Inc. is recalling the Zimmer Dermatome AN (Model 88710100), a surgical device used to remove thin layers of skin. The device may have a misaligned thickness control bar that could affect its operation. This is a Class I recall, the most serious classification, and affects all units of this model.
- Recalling firm
- Zimmer Surgical Inc
- Product
- Zimmer Dermatome AN, Model/Catalog Number: 88710100
- Reason
- The devices may have a misaligned thickness control bar.
- Classification
- Class I
- Category
- consumer product recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2025-11-24
- Status
- Open, Classified
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/f14ad13c-7bfc-47d4-b6b2-edaf658fc64a