Class II
Medical Device Recall: Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Schiller, Ag · August 8, 2025
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.
States Affected
NATIONWIDE
Quantity Affected
266 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2672-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.