Drug recall
Philips Efficia CMS200 Central Monitoring System; 863352 The Efficia CMS200 central monitoring system is…
FDA recall event 76274 · Class II · Philips Electronics North America Corporation
Key facts
| Event ID | 76274 |
|---|---|
| Recall numbers | Z-1229-2017 |
| Recalling firm | Philips Electronics North America Corporation |
| Product type | Devices |
| Products | Philips Efficia CMS200 Central Monitoring System; 863352 The Efficia CMS200 central monitoring system is intended for use by healthcare professionals for central viewing of physiologic waves… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The monitor may not alarm appropriately for a pediatric or neonatal patient. |
| Initiation date | Jan 17, 2017 |
| Report date | Mar 1, 2017 |
| Termination date | Oct 10, 2019 |
| 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: