Biodesign Fistula Plug C-FPB-0.7 - For implantation to reinforce soft tissue for repair of recto-...

FDA Recall #Z-3251-2024 — Class II — August 7, 2024

Recall #Z-3251-2024 Date: August 7, 2024 Classification: Class II Status: Ongoing

Product Description

Biodesign Fistula Plug C-FPB-0.7 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN): G24668

Reason for Recall

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

Recalling Firm

Cook Biotech, Inc. — W Lafayette, IN

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

3 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.

Code Information

UDI-DI: (01)00827002246683(17)250605(10)LB1536090 (01)00827002246683(17)250627(10)LB1536126 Lot Number: LB1536090, LB1536126

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated