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W.H.P.M. INC. · Model W15134 · UDI-DI 00841824105102

JXN DKZ DIS JXM DIO LAF DJR DJG LCM LDJ LFG Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

DOA 13 in 1 Test Dip Card, 25Pcs/Box, CLIA Waived, AMP/BARB/BUP/BZO/COC/mAMP/MTD/OPI/OXY/PCP/PPX/TCA/THC

Recalls

Date	Firm	Reason
2010-10-04	Express Diagnostics Int'l., Inc.	Express Diagnostics Int'l, Inc (EDI), is recalling DrugCheck Drug Screen Cups containing buprenorphine (BUP) and propoxyphene (PPX) because they must be labeled as "forensic use o
2008-05-28	Sun Biomedical Laboratories, Inc.	Product was sold while the devices were under FDA 510 (k) review, which was subsequently denied.

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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.