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ArgoTrans Model 1

ARGON MEDICAL DEVICES, INC. · Model 041517504A · UDI-DI 00886333201655

DRS Prescription
10
510(k) clearances
3,904
Adverse events (25 deaths)
236
Recalls
86
Facilities

Description

ArgoTrans Model 1 w/ 42" Cable, 1 Way Stopcock

Recalls

DateFirmReason
2026-03-24Medline Industries, LPMedline has identified the presence of particulate within the fluid path of the Manifolds.
2026-03-24Medline Industries, LPMedline has identified the presence of particulate within the fluid path of the Manifolds.
2025-02-12MEDLINE INDUSTRIES, LP - NorthfieldThe female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
2023-11-10Smiths Medical Asd IncThere is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inad
2023-11-10Smiths Medical Asd IncThere is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inad
2023-11-10Smiths Medical Asd IncThere is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inad
2023-11-10Smiths Medical Asd IncThere is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inad
2023-11-10Smiths Medical Asd IncThere is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inad
2023-11-10Smiths Medical Asd IncThere is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inad
2023-11-10Smiths Medical Asd IncThere is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inad

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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.