FDA Device Intelligence
Home › JANT PHARMACAL CORPORATION › accutest®

accutest®

JANT PHARMACAL CORPORATION · Model DS106 · UDI-DI 10763924106629

LFGLDJLCMJXNJXMDKZDJRDJGDJCDISDIO
10
510(k) clearances
8
Adverse events
2
Recalls
49
Facilities

Description

ACCUTEST MultiDrug Screen-10+6 (AMP/BARB/BZD/COC/MTDN/M-AMP/OPI/PCP/TCA/THC) w/Adulteration Screen (pH/ S.G./ Oxidant/Nit/Glut/Creatinine)

Recalls

DateFirmReason
2026-06-26Siemens Healthcare Diagnostics, Inc.out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2. While the assay results were not impacted, the overall h
2003-11-17Abbott Health Products, Inc.Drug product cross reacts with the Tricyclic Antidepressants (TCA) assay.

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.