PulseOne has recalled a batch of home blood pressure monitors because a firmware issue can cause readings to display lower than actual, which may delay needed care.
What was recalled
The recall covers PulseOne Home BP Monitor model PO-BP2.
Products and models affected
- Model PO-BP2 (upper-arm monitor)
- Firmware versions 1.02 and 1.03
- Serial numbers beginning PO2-24
The model and serial number are on the back of the device; firmware appears on the startup screen.
Why it was recalled
Under-reporting blood pressure can lead users and their doctors to underestimate risk. PulseOne has received 7 reports of inconsistent readings; no injuries confirmed.
What you should do
Stop relying on the device for medical decisions and contact your healthcare provider if you have concerns.
Free Replacement
PulseOne is providing a free replacement monitor with corrected firmware and a prepaid return label for the affected unit.
Important dates & details
- Units affected: ~26,000
- Sold: 2024 – 2025
- Price: $39–$59
- Incidents: 7 inaccurate-reading reports
Official Source
U.S. Food and Drug Administration (FDA) — View the official recall notice. Verify all details and file any claim directly through the official source.