SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1963
Class I - Dangerous 🏥 Medical Devices
Recalled: June 11, 2024 Ethicon Sarl, a Johnson & Johnson Company Other Medical Devices
Nationwide
What Should You Do?
- Check if you have this product: Product Number: 1963; UDI/DI: 10705031003132 (primary), 20705031003139 (box of 10); Lot numbers:
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Ethicon Sarl, a Johnson & Johnson Company
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1963
Product Codes/Lot Numbers:
Product Number: 1963; UDI/DI: 10705031003132 (primary), 20705031003139 (box of 10); Lot numbers:
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2407-2024
Related Recalls
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1961
Ethicon Sarl, a Johnson & Johnson Company
Class I - Dangerous
Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.