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

Recall Z-0814-2022 — TCL1 Breakapart Probe, Fluorescence in situ hybridisation (FISH) is a technique allows the visualisation of DNA sequences upon chromosome Catalog Number: LPH046-A

U.S. FDA — Device Enforcement · United Kingdom · 2022-02-04 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0814-2022
Date of alert
2022-02-04
Country / jurisdiction
United Kingdom
Risk level
Class III
Risk type
recall
Brand
Cytocell Ltd.
Product category
device
Product type
Devices
Reported risk: May show unexpected locus specific signals in addition to those at 14q32.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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