PlainRecalls
FDA Devices Moderate Class II Ongoing

Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues in the inguinal floor to repair inguinal hernias. Order Number (GPN): G46603

Reported: October 2, 2024 Initiated: August 7, 2024 #Z-3261-2024

Product Description

Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues in the inguinal floor to repair inguinal hernias. Order Number (GPN): G46603

Reason for Recall

Products expire prior to the expiration date printed on the product labeling

Details

Recalling Firm
Cook Biotech, Inc.
Units Affected
120 units
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Austria, Canada, China, Finland, France, Germany, Ireland, Luxembourg, Netherlands, New Zealand, Norway, South Africa, United Kingdom.
Location
W Lafayette, IN

Frequently Asked Questions

What product was recalled?
Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues in the inguinal floor to repair inguinal hernias. Order Number (GPN): G46603. Recalled by Cook Biotech, Inc.. Units affected: 120 units.
Why was this product recalled?
Products expire prior to the expiration date printed on the product labeling
Which agency issued this recall?
This recall was issued by the FDA Devices on October 2, 2024. Severity: Moderate. Recall number: Z-3261-2024.