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.

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.