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

Recall Z-1202-2019 — Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent.

U.S. FDA — Device Enforcement · United Kingdom · 2019-03-15 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1202-2019
Date of alert
2019-03-15
Country / jurisdiction
United Kingdom
Risk level
Class III
Risk type
recall
Brand
Cytocell Ltd.
Product category
device
Product type
Devices
Reported risk: There is an error in the chromomap included in the labeling for the product.
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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