Zimmer Dermatome AN — Class II medical device recall Z-0925-2026
Ongoing recall by Zimmer Surgical Inc, reported 2025-12-24. The devices may have a misaligned thickness control bar.
| Recall number | Z-0925-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Surgical Inc, Dover, OH, United States |
| Recall initiated | 2025-11-24 |
| Classified | 2025-12-15 |
| Reported by FDA | 2025-12-24 |
| Countries outside the US | AU, CA, CN, GT, HK, IN, JP, KR, MX, MY, PA, SG, TH, TT, TW |
| Quantity | 498 units |
| Lot numbers | 65900465, 65944825, 66016265, 66121190, 66121191, 66252848, 66252849, 66252850, 66342488, 66531526, 66531527, 66531528, 66531529, 66609571, 66620981, 66620983, 66751092, 66751093, 66849858, 66849859, 66995362, 67025608, 67044648, 67080990, 67198242, 67198243, 67198249, 67214429, 67277943 |
| Serial numbers | 701341, 701343, 701344, 701345, 701346, 701350, 701351, 701352, 701353, 701354, 701355, 701356, 701357, 701359, 701361, 701362, 701363, 701364, 701365, 701366, 701367, 701368, 701369, 701370, 701371 and 475 more |
| Model numbers | 88710100 |
Product
Zimmer Dermatome AN, Model/Catalog Number: 88710100
Reason for recall
The devices may have a misaligned thickness control bar.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0925-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.