Ethicon Sarl, a Johnson & Johnson Company: Device Recall
Recall #Z-2407-2024 · 06/11/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2407-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Ethicon Sarl, a Johnson & Johnson Company
- Status
- Ongoing
- Date Initiated
- 06/11/2024
- Location
- Neuchatel, Switzerland
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 39,010 units (All US)
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.
Product Description
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1963
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of India and Japan.
Other Recalls by Ethicon Sarl, a Johnson & Johnson Company
- Class II: Risk 06/11/2024
View all recalls by Ethicon Sarl, a Johnson & Johnson Company →
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.