FDA Device recall Z-1896-2026
Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm
- FDA Device
- Class II
- ongoing
- Published 2026-04-29
On 2026-04-29 the FDA classified a Class II recall of Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm by Davol, citing potential for product to contain foreign matter, confirmed to be inspect fragments.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1896-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-03-25 |
| Published | 2026-04-29 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Davol |
| Distribution | US |
Product
Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.
Reason
Potential for product to contain foreign matter, confirmed to be inspect fragments.
Identifiers
| code_info | Catalog Number: 1050030. UDI: (01)00801741010538(17)270728(10)WBJS0055. Lot Number: WBJS0055. Expiration Date: 07/28/2027 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1896-2026%22
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