SURGICEL FIBRILLAR 1INX2IN — Class II medical device recall Z-2407-2024
Ongoing recall by Ethicon Sarl, a Johnson & Johnson Company, reported 2024-07-24, distributed nationwide. Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine u
| Recall number | Z-2407-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ethicon Sarl, a Johnson & Johnson Company, Neuchatel, Switzerland |
| Recall initiated | 2024-06-11 |
| Classified | 2024-07-17 |
| Reported by FDA | 2024-07-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | IN, JP |
| Quantity | 39,010 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10705031003132, 20705031003139 |
Product
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1963
Reason for recall
Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.
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-2407-2024. 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.