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CytoCell

CYTOCELL LIMITED · Model USA-LPH024 · UDI-DI 05055844905924

QDI Prescription
1
510(k) clearances
0
Adverse events
1
Recalls
2
Facilities

Description

Del(5q) Deletion FISH Probe Kit

Recalls

DateFirmReason
2022-01-18Cytocell Ltd.individual components have been labelled with incorrect colours. The red and green colours are opposite to those specified in the product labelling. The EGR1 probe is labelled in g

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.