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

Recall Z-0360-2020 — Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) - Product Usage: The catheterization table is used with Infinix-8000F System (Interventional Angiography System), to position patient during diagnostic and interventional x-ray angiography.

U.S. FDA — Device Enforcement · United States · 2019-02-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0360-2020
Date of alert
2019-02-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Canon Medical System, USA, INC.
Product category
device
Product type
Devices
Reported risk: Table tilts without operator involvement as a result of liquid spilling into tilt console triggering a short circuit.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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