Health & Personal Care
HIGH
FDA DEVICE
Schiller Argus PB-3000 Vital Signs Monitor Recall Affects 266 US Units
Schiller, AG recalls 266 Argus PB-3000 vital sign monitors nationwide in the United States. The devices may display an error message during blood pressure measurements when the initial inflation pressure is set high. Authorities urge users to stop using the device and follow manufacturer instructions.
Schiller
Vital sign