FDA Device recall Z-2829-2018
Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
- FDA Device
- Class II
- completed
- Published 2018-08-22
On 2018-08-22 the FDA classified a Class II recall of Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive by Withings Sas, citing device could not meet the requirements for systolic pressure.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2829-2018 |
| Classification | Class II |
| Status | completed |
| Initiated | 2018-06-11 |
| Published | 2018-08-22 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Withings Sas |
| Distribution | US |
Product
Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
Reason
Device could not meet the requirements for systolic pressure
Identifiers
| code_info | 7024260310 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2829-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.