FDA Device recall Z-2407-2024
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1963
- FDA Device
- Class II
- ongoing
- Published 2024-07-24
On 2024-07-24 the FDA classified a Class II recall of SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1963 by Ethicon Sarl A Johnson And Johnson, citing some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2407-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-06-11 |
| Published | 2024-07-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Ethicon Sarl A Johnson And Johnson |
| Distribution | US |
Product
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1963
Reason
Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.
Identifiers
| code_info | Product Number: 1963; UDI/DI: 10705031003132 (primary), 20705031003139 (box of 10); Lot numbers: |
|---|
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-2407-2024%22
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