Drug recall
Spacelabs Ultraview DM3 Monitor Model Number: 91330-NT The Ultraview DM3 Monitor is indicated for use by…
FDA recall event 62939 · Class II · Zoe Medical Incorporated
Key facts
| Event ID | 62939 |
|---|---|
| Recall numbers | Z-2380-2012 |
| Recalling firm | Zoe Medical Incorporated |
| Product type | Devices |
| Products | Spacelabs Ultraview DM3 Monitor Model Number: 91330-NT The Ultraview DM3 Monitor is indicated for use by health care professionals for monitoring patient vital signs. The Ultraview DM3 Monitor is… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Unit fails to power up, resulting in an equipment alarm |
| Initiation date | Jun 6, 2012 |
| Report date | Sep 26, 2012 |
| Termination date | Sep 18, 2012 |
| City | Topsfield |
| State | MA |
| Country | United States |
| FEI number | 3003294644 |
At a glance
- 1–9 Products in this recall
- 1–9 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: