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INSTI HIV-1 Control Test Kit

Biolytical Laboratories Inc · Model 90-1030 · UDI-DI 00686597010303

MZF
0
510(k) clearances
3,206
Adverse events (4 deaths)
1
Recalls
37
Facilities

Description

INSTI HIV-1 Control Test Kit

Recalls

DateFirmReason
2025-04-24Mckesson Medical-Surgical Inc. Corporate Officetransit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failur

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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.