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

Recall Z-1195-2014 — CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS ANALYZER II¿ is a semi-automated fluorescence microscope, consisting of the analyzer, a dedicated computer with CELLTRACKS¿ software, monitor, keyboard, mouse and uninterruptible power supply (UPS). The system also suppo

U.S. FDA — Device Enforcement · United States · 2014-01-08 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1195-2014
Date of alert: 2014-01-08
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Veridex, LLC
Product category: device
Product type: Devices

Reported risk: Janssen Diagnostics, LLC received complaints of camera failures on the CELLTRACKS ANALYZER II¿.

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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