FDAAugust 8, 2025device
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Official recall recorded by the U.S. Food & Drug Administration.
The 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.
What to do
FDA enforcement status: Ongoing
Brands named
schiller agschillerschiller ag
UPCs
0761336500302407613365001914076133650034680761336500347507613365000115
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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