3:1 Dermacarrier — Class II medical device recall Z-1078-2024
Ongoing recall by Zimmer Surgical Inc, reported 2024-02-21, distributed nationwide. Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The p
| Recall number | Z-1078-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Surgical Inc, Dover, OH, United States |
| Recall initiated | 2024-01-02 |
| Classified | 2024-02-13 |
| Reported by FDA | 2024-02-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, HK, IN, JP, KR, MX, NL, SG, TH, TW |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00889024378780 |
| Lot numbers | 65292843 |
| Model numbers | 00219501300 |
| Expiration dates | 2026-10-16, 2027-01-18 |
Product
3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
Reason for recall
Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The problem may lead to minor tissue damage or additional unplanned graft if deemed necessary.
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-1078-2024. 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.