FDA Device recall Z-1078-2024
3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
- FDA Device
- Class II
- ongoing
- Published 2024-02-21
On 2024-02-21 the FDA classified a Class II recall of 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier by Zimmer Surgical, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1078-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-01-02 |
| Published | 2024-02-21 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Zimmer Surgical |
| Distribution | US |
Product
3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
Reason
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.
Identifiers
| code_info | UDI-DI 00889024378780 Lots 65292843 (Expires 16-Oct-2026) and 65390419 (Expires 18-Jan-2027) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1078-2024%22
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