Drug recall
Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275, 863276, 863277, VS2+ 863278…
FDA recall event 62865 · Class II · Philips Healthcare Inc.
Key facts
| Event ID | 62865 |
|---|---|
| Recall numbers | Z-2303-2012 |
| Recalling firm | Philips Healthcare Inc. |
| Product type | Devices |
| Products | Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275, 863276, 863277, VS2+ 863278, 863279. The SureSigns VS2+ vital signs monitor is for monitoring, recording and alarming of… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and may fall from the wall mount |
| Initiation date | Aug 15, 2012 |
| Report date | Sep 5, 2012 |
| Termination date | Mar 13, 2014 |
| City | Andover |
| State | MA |
| Country | United States |
| FEI number | 1218950 |
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: