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DrugSmart Cup

CHEMTRON BIOTECH INC · Model 61060D-6AB · UDI-DI 00812203030780

LCM DJC DIS JXM LDJ LAF DIO DKZ DJG LFG Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

DrugSmart Cup 10, AMP/BAR/BZO/COC/MDMA/MET/OPI2K/PCP/TCA/THC + (Cr/SG/Ox)(Ni/pH/Gl)

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.