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Identify®Diagnostics Drug Test Cups

MEDICAL DISTRIBUTION GROUP INC · Model ID-CP12-BUP-ADULT-AZ10 · UDI-DI 10850013035110

LCM DJC DJR DIS JXM DIO DJG LDJ DKZ Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Identify® Diagnostics Drug Test Cups 12-Panel Drug Screening Test Cup AMP/BAR/BUP/BZO/COC/MTD/MDMA/MET/MOP/OXY/PCP/THC with Adulteration strip (S.G./CRE/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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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.