FDA Device Intelligence
Home › ARK DIAGNOSTICS INC › ARK™ Methotrexate II Control

ARK™ Methotrexate II Control

ARK DIAGNOSTICS INC · Model 5071-0003-02 · UDI-DI 00812101031216

LAO Prescription
1
510(k) clearances
20
Adverse events
2
Recalls
4
Facilities

Description

ARK™ Methotrexate II Control is intended for use in quality control of the ARK Methotrexate II Assay.

Recalls

DateFirmReason
2016-03-08Siemens Healthcare Diagnostics, Inc.Siemens Healthcare Diagnostics confirmed that Syva Emit Methotrexate Application (DVMTX.1) for Dimension Vista System does not meet On-Board Stability claim of 20 hours. Testing us
2007-03-20Abbott Diagnostic International, Ltd.Incorrect configuration: kits contain reagent bottles in the order S-W-T-P instead of the correct order, W-S-T-P.

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.