Ethicon, Inc.: Device Recall
Recall #Z-2144-2024 · 05/10/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2144-2024
- 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
- 341532 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 (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic surgery, but not for use in cardiovascular and neurological tissues. PRODUCT CODE: J214H J218H J258H J268H J269H J327H J344H J345H J370H J416H J417H J426H J427H J458H J493H J603H J699H J936H J978H
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.