HIGHFDA DEVICE
Schiller Ag Recalls Argus PB-3000 Due to Error Message Hazard
Schiller Ag recalled 266 units of the Argus PB-3000 on August 8, 2025. The vital sign monitoring instrument may trigger an error message during blood pressure measurements. The recall affects devices distributed nationwide in Montana, Wisconsin, and Illinois.
Schiller, Ag
Vital sign