Nokia BPM+ Wireless Blood Pressure Monitor Product System — Class II medical device recall Z-2829-2018
Completed recall by Withings Sas, reported 2018-08-22, distributed nationwide. Device could not meet the requirements for systolic pressure
| Recall number | Z-2829-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Withings Sas, Issy les Moulineaux, France |
| Recall initiated | 2018-06-11 |
| Classified | 2018-08-16 |
| Reported by FDA | 2018-08-22 |
| Distributed | Nationwide (US) |
Product
Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
Reason for recall
Device could not meet the requirements for systolic pressure
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2829-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.