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.

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.