FDA Device recall Z-0925-2026
Zimmer Dermatome AN, Model/Catalog Number: 88710100
- FDA Device
- Class II
- ongoing
- Published 2025-12-24
On 2025-12-24 the FDA classified a Class II recall of Zimmer Dermatome AN, Model/Catalog Number: 88710100 by Zimmer Surgical, citing the devices may have a misaligned thickness control bar.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0925-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-11-24 |
| Published | 2025-12-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Zimmer Surgical |
| Distribution | n/a |
Product
Zimmer Dermatome AN, Model/Catalog Number: 88710100
Reason
The devices may have a misaligned thickness control bar.
Identifiers
| code_info | Lot Code: Model No 88710100, UDI 00889024464834701341, Lot Number 65900465, Serial Number 701341; Model No 88710100, UD…Lot Code: Model No 88710100, UDI 00889024464834701341, Lot Number 65900465, Serial Number 701341; Model No 88710100, UDI 00889024464834701343, Lot Number 65900465, Serial Number 701343; Model No 88710100, UDI 00889024464834701344, Lot Number 65900465, Serial Number 701344; Model No 88710100, UDI 00889024464834701345, Lot Number 65900465, Serial Number 701345; Model No 88710100, UDI 00889024464834701346, Lot Number 65900465, Serial Number 701346; Model No 88710100, UDI 00889024464834701350, Lot Number 65900465, Serial Number 701350; Model No 88710100, UDI 00889024464834701351, Lot Number 65900465, Serial Number 701351; Model No 88710100, UDI 00889024464834701352, Lot Number 65900465, Serial Number 701352; Model No 88710100, UDI 00889024464834701353, Lot Number 65900465, Serial Number 701353; Model No 88710100, UDI 00889024464834701354, Lot Number 65900465, Serial Number 701354; Model No 88710100, UDI 00889024464834701355, Lot Number 65900465, Serial Number 701355; Model No 88710100, UDI |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
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FDA Device · Class II · 2025-12-24 · Zimmer Surgical
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0925-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.