Ethicon, Inc.: Device Recall
Recall #Z-2145-2024 · 05/10/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2145-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Ethicon, Inc.
- Status
- Ongoing
- Date Initiated
- 05/10/2024
- Location
- Raritan, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 55296 units
Reason for Recall
Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection .
Product Description
VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, except for ophthalmic, cardiovascular and neurological tissues. PRODUCT CODE: VCP196H VCP417H VCP602H VCP603H VCP662H VCPB259H VCPB946H
Distribution Pattern
Worldwide distribution - US Nationwide including PR and the countries of AR, AU, AU, BE, BR, CA, CA, CL, CN, CO, CR, EC, IL, JP, JP, KW, MX, NZ, PA, PR, PR, SA, SG, UY, ZA.
Other Recalls by Ethicon, Inc.
- Class II: Risk 10/08/2024
- Class II: Risk 09/25/2024
- Class II: Risk 05/10/2024
- Class II: Risk 05/10/2024
- Class II: Risk 05/10/2024
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.