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

Recall date

August 8, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2672-2025

FDA classification

Class II

Brand / firm

Schiller, Ag

Sold / distributed

US Nationwide distribution in the states of MT, WI, IL.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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