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IDS ACTH II

IMMUNODIAGNOSTIC SYSTEMS LIMITED · Model IS-4500NG · UDI-DI 05060169696457

CKG Prescription
1
510(k) clearances
33
Adverse events
6
Recalls
20
Facilities

Recalls

DateFirmReason
2025-11-03GET TESTED INTERNATIONAL ABDistribution without premarket approval/clearance.
2025-11-03GET TESTED INTERNATIONAL ABDistribution without premarket approval/clearance.
2025-11-03GET TESTED INTERNATIONAL ABDistribution without premarket approval/clearance.
2018-11-30Tosoh Bioscience Inc
2011-12-13Beckman Coulter Inc.The recall was initiated because Beckman Coulter has confirmed that the DxH Slidemaker Stainer Floor Stand shipped with Slidemaker Stainer instruments were missing vinyl caps, expo
2005-04-22Nichols Institute DiagnosticsPerformance does not meet claims in the Directional Insert concerning correlation with the IRMA ACTH 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.