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

Recall Z-1640-2021 — 8G DIRECT WORKING CANNULA BEVEL TIP, CODE INTVM-DWCB

U.S. FDA — Device Enforcement · Italy · 2021-03-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1640-2021
Date of alert
2021-03-22
Country / jurisdiction
Italy
Risk level
Class II
Risk type
recall
Brand
BIOPSYBELL S.R.L.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
20061432
Reported risk: Products labeled as sterile were distributed, but may not have been sterilized.
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.