Ethicon, Inc.: Device Recall
Recall #Z-2149-2024 · 05/10/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2149-2024
- 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
- 287892 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
MONOCRYL Plus Antibacterial (poliglecaprone 25) Suture - Intended for use in general soft tissue approximation and/or ligation where an absorbable material is indicated. PRODUCT CODE: MCP266H13 MCP3200H16 MCP3212H16 MCP3213H16 MCP340H13 MCP345H13 MCP416H14 MCP417H14 MCP426H13 MCP427H13 MCP4423H16 MCP4424H14 MCP442H14 MCP496H16 MCP497H16 MCP604H13 MCP936H13 MCP945H14 MCPB346H13
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.