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QwikCheck Liquefaction

M.E.S. MEDICAL ELECTRONIC SYSTEMS LTD. · Model QwikCheck Liquefaction- 20 Vials · UDI-DI 07290012140150

IBG Prescription
2
510(k) clearances
0
Adverse events
1
Recalls
12
Facilities

Recalls

DateFirmReason
2018-08-02Ventana Medical Systems IncLeaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.

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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.