Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-3251-2024 — 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

U.S. FDA — Device Enforcement · United States · 2024-08-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3251-2024
Date of alert
2024-08-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cook Biotech, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00827002246683
Reported risk: Products expire prior to the expiration date printed on the product labeling
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.