Zimmer Air Dermatome — Class II medical device recall Z-0924-2026
Ongoing recall by Zimmer Surgical Inc, reported 2025-12-24. The devices may have a misaligned thickness control bar.
| Recall number | Z-0924-2026 |
|---|---|
| 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 | 839 units |
| UPC / GTIN / UDI-DI | 00889024375901 |
| Lot numbers | 65944745, 65944748, 65944750, 65944752, 66053364, 66053365, 66121180, 66121181, 66121182, 66121183, 66121184, 66185343, 66185344, 66185345, 66252794, 66252795, 66360518, 66360519, 66427989, 66428246, 66472343, 66488262, 66531522, 66531523, 66531525, 66588831, 66588832, 66609568, 66609569, 66609570, 66620922, 66620923, 66620924, 66694114, 66694115, 66694116, 66799187, 66799188, 66847657, 66847658 and 18 more |
| Serial numbers | 115821, 115824, 115826, 115827, 115829, 115831, 115832, 115834, 115835, 115836, 115838, 115839, 115841, 115842, 115843, 115845, 115846, 115847, 115848, 115850, 115853, 115854, 115855, 115856, 115857 and 475 more |
| Model numbers | 0088010010, 00880100100 |
Product
Zimmer Air Dermatome, Model/Catalog Number: 00880100100
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-0924-2026. 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.