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.

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.