SURGICEL FIBRILLAR 1INX2IN — Class II medical device recall Z-2406-2024
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-2406-2024 |
|---|---|
| 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 |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10705031003118, 20705031003115 |
| Lot numbers | RME2541, RPE3181, RPE3591, SBB2291, SDB5001, SHB9841, SJB9871, SJE0231, SJE0241, SJE0361, SKE1781, SKE1791, SKE1801, SKE1811, SKE2101, SKE2111, SKE2201, SLE4411, TBB1511, TBB1661, TBB2481, TBB2491, TCB2931, TCB3341, TCB3351, TCB3751, TCB3781, TCB4051, TCB4061, TCB4071, TCB4081, TCB4471, TCB4481, TDB5151, TDB5611, TDB5621, TDB5631, TDB5981, TDB5991, TDB6001 and 21 more |
Product
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1961
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-2406-2024. 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.