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T-Cube

WONDFO USA CO., LTD. · Model ODOA-856EUO · UDI-DI 00816862021998

LCM DJG LAF DIO DKZ Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

5-Panel T-Cube; AMP,COC,MET,OPI,PCP

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.