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Wondfo Drug Test Dip Card

WONDFO USA CO., LTD. · Model WDMA-114 · UDI-DI 00816862020458

LAF Prescription
1
510(k) clearances
0
Adverse events
1
Recalls
65
Facilities

Description

1-Panel Card; mAMP/MET Methamphetamine

Recalls

DateFirmReason
2021-02-05OraSure Technologies, Inc.Incorrect lot of Substrate Reagent (TMB) may be included in the kit. The original kit box labeling and the specification sheet listed the Substrate Reagent (TMB) lot 6676239, but

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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.