Drug recall
Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
FDA recall event 80533 · Class II · Withings Sas
Key facts
| Event ID | 80533 |
|---|---|
| Recall numbers | Z-2829-2018 |
| Recalling firm | Withings Sas |
| Product type | Devices |
| Products | Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Device could not meet the requirements for systolic pressure |
| Initiation date | Jun 11, 2018 |
| Report date | Aug 22, 2018 |
| City | Issy les Moulineaux |
| Country | France |
| FEI number | 3012024804 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: