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

Recall Z-0676-2024 — BD Recanalization System, REF: BDRECANSYSTEM

U.S. FDA — Device Enforcement · United States · 2023-11-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0676-2024
Date of alert
2023-11-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Bard Peripheral Vascular Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00801741202421
Reported risk: Recanalization systems may be in a manufacturing mode that allows the system to continuously run without the typical 30 second pauses, and 4-minute warning/5-minute restart required messages to indicate the ten-minute maximum catheter use time has been exceeded, which may increase the risk of the device overheating or breaking.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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