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Express ResultsTM

Quest Diagnostics · Model DOA-154-181 · UDI-DI 20869419000247

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

Description

DOA-154-181(COC/AMP/THC/OPI/PCP)MULTI-DRUG 5 PANEL SCREEN TEST (DOA-154-181) previous (GTIN 10869419000240)

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.

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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.