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AmediCheck Instant Test Cup

AMEDITECH INC. · Model C-C0601A-3A · UDI-DI 00816565020533

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510(k) clearances

Adverse events

Recalls

Facilities

Description

THC, COC, OPI, AMP, MET, PCP with Adulteration Screen for OX/SG/PH

Recalls

Date	Firm	Reason
2005-05-31	Applied Biotech Inc	The firm has discovered that a number of distributed devices of the Medplus ER Drug Screen Test may be incorrectly assembled which may give incorrect results. The product is an in

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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.