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Noble 1 Step Cup

NOBLE MEDICAL INC · Model NBCA-14A-PP · UDI-DI 00858886006322

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

510(k) clearances

Adverse events

Recalls

Facilities

Description

Drugs of Abuse Test Cup for THC50/C0C150/0PI300/mAMP500/AMP500/BZO300/BAR300/MTD300/MDMA500/OXY100/BUP10/TCA1000/PPX300/PCP25 + (Creatinine/Ni/pH/B1/S.G.)

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.