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

Recall Z-2326-2020 — Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the

U.S. FDA — Device Enforcement · United States · 2020-03-03 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2326-2020
Date of alert: 2020-03-03
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: Bolts holding the longitudinal movement of catheterization tables may be loose, which may lead to table surface/top tilting.

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.

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