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Rapid Response

BTNX Inc · Model D10.43-1P29-25 · UDI-DI 10722066008253

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1
510(k) clearances
0
Adverse events
1
Recalls
50
Facilities

Description

Rapid Response Single/Multi DOA Panel MOR 2000 (Urine)- OXY100, MDMA500, COC300, BZO300, EDDP300, BUP10, MET1000, OPI2000, AMP1000, THC50-25 tests/ kit

Recalls

DateFirmReason
2017-09-30Ameditech IncProduct was released to market without the adulteration strip included in the product.

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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.