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SICU ANESTHESIA SET

ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Model 687100 · UDI-DI 00886333671007

DXN Prescription
10
510(k) clearances
3,169
Adverse events (16 deaths)
36
Recalls
429
Facilities

Description

A single 3cc transducer connected to a 20 drops, 60" tube Adset. The patient line is connected with a 48" pressure tube and a 12" pressure tube via 3-way White stopcocks.

Recalls

DateFirmReason
2025-02-24PYRAMES INCSingle-use battery-powered blood pressure monitor, for use on neonates and infants, due to vibratory noise, may not adequately detect changes in blood pressure per specification. C
2024-08-30MEDLINE INDUSTRIES, LP - NorthfieldIt has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as
2024-08-30MEDLINE INDUSTRIES, LP - NorthfieldIt has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as
2024-08-30MEDLINE INDUSTRIES, LP - NorthfieldIt has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as
2024-03-26Baxter Healthcare CorporationBaxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical s
2024-03-26Baxter Healthcare CorporationBaxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical s
2024-03-26Baxter Healthcare CorporationBaxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical s
2024-02-26MEDLINE INDUSTRIES, LP - NorthfieldThe firm provided a set of specifications for the device, but some units of the device were manufactured non-compliant with the specifications. However, the firms Receiving Dept. a
2021-05-17Mediana Co., Ltd.In some cases the equipment fails to power up and/or key or button unresponsive or not working.
2021-04-22Welch Allyn IncPotential Risk of fluid ingress to the power supplies, resulting in risk of an internal electrical short and possible electrical shock

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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.