FDA Device Intelligence
Home › TRANSMED CO, LLC › CSI

CSI

TRANSMED CO, LLC · Model CSI-CUP-1145S · UDI-DI 00850798007787

JXNLFGLCMLDJDJRLAFDIODJGJXMDISDKZ Prescription
10
510(k) clearances
1
Adverse events
2
Recalls
55
Facilities

Description

CSI Cup - CLIA Screen In-Vitro 14 Panel Drug Test, Click Seal Cap, AMP500, BAR, BUP, BZO, COC150, mAMP500, MDMA, MOP300, MTD, OXY, PCP, PPX, TCA, THC, 25/BX

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.