Zimmer Air Dermatome II — Class II medical device recall Z-1485-2013
Terminated recall by Zimmer Surgical Inc, reported 2013-06-12, distributed nationwide. This removal is in response to complaints alleging that the Zimmer Air Dermatomes and Zimmer Air Dermatome II
| Recall number | Z-1485-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Surgical Inc, Dover, OH, United States |
| Recall initiated | 2013-05-07 |
| Classified | 2013-06-05 |
| Reported by FDA | 2013-06-12 |
| Terminated | 2014-12-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, CL, CN, DE, EG, GB, HK, JP, KR, SE, SG, TH, TW |
| Quantity | 13 units |
| Serial numbers | 500311, 500312, 500317, 500320, 500321, 500322, 500323, 500324, 500325, 500326, 500327, 500328, 500329 |
| Model numbers | 00-8851-001-01 |
Product
Zimmer Air Dermatome II, REF 00-8851-001-01 handpiece, w/o hose, Rx, non-sterile grafting instruments intended to provide variable graft thickness and width capabilities.
Reason for recall
This removal is in response to complaints alleging that the Zimmer Air Dermatomes and Zimmer Air Dermatome II products would either not operate or operate intermittently. Zimmer's investigation determined that the planetary gear teeth were broken. This may cause a delay or postponement of the surgery or result in a suboptimal graft retrieval with potential of requiring an additional donor site.
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-1485-2013. 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.