Withings Sas: Medical Device Recall in 2018 - (Recall #: Z-2829-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive

Product Classification:

Class II

Date Initiated: June 11, 2018

Date Posted: August 22, 2018

Recall Number: Z-2829-2018

Event ID: 80533

Reason for Recall:

Device could not meet the requirements for systolic pressure

Status: Completed

Product Quantity: Total 44,000 units (15,139 US/ 28,861 OUS)

Code Information:

7024260310

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated