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FDA (Device enforcement)Recalled 2025-08-08class ii

Schiller, Ag: Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006

Hazard

Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.

Details from the source

Reason for recall: Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range. Distribution: US Nationwide distribution in the states of MT, WI, IL. Quantity: 266 units Lot/code info: REF: 1A.701307: UDI- 07613365003024 REF: 3.921002, UDI: 07613365001914 REF: 3.921030, UDI: 07613365003468 REF: 3.921031: UDI: 07613365003475 REF: 3.921006, UDI: 07613365000115 Affected Serial Numbers: 7010.000160 and lower, 7012.000356 and lower, 7013.000256 and lower, 7014.000152 and lower

UPC codes

07613365003024, 07613365001914, 07613365003468, 07613365003475, 07613365000115

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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