FDA Device Intelligence
Home › UCP BIOSCIENCES, INC. › UCP Home Drug Screening Test Cards

UCP Home Drug Screening Test Cards

UCP BIOSCIENCES, INC. · Model U-DOA-3124 · UDI-DI 10817038021474

JXNLFGLDJLCMDJRDJCDIODJGJXMDISDKZ Prescription
2
510(k) clearances
1
Adverse events
2
Recalls
55
Facilities

Description

UCP Home Drug Screening Test Cards 12 Panel Drug Test Card BZO/BAR/COC/THC/mAMP/MOP/MTD/TCA/OXY/MDMA/PCP/AMP

Recalls

DateFirmReason
2010-10-04Express 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
2008-05-28Sun Biomedical Laboratories, Inc.Product was sold while the devices were under FDA 510 (k) review, which was subsequently denied.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.