Drug recall
Perseus A500 Anesthesia Workstation, MK06000. Intended for use in anesthetizing adults, children, and neonates…
FDA recall event 72649 · Class I · Draeger Medical, Inc.
Key facts
| Event ID | 72649 |
|---|---|
| Recall numbers | Z-0360-2016 |
| Recalling firm | Draeger Medical, Inc. |
| Product type | Devices |
| Products | Perseus A500 Anesthesia Workstation, MK06000. Intended for use in anesthetizing adults, children, and neonates and can be used for automatic and manual ventilation, pressure-supported spontaneous… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | There is a potential problem with the device main power switch of the Perseus A500 Anesthesia Workstation. The device power switch may spontaneously fail during use, causing one of the following to… |
| Initiation date | Nov 12, 2015 |
| Report date | Dec 23, 2015 |
| Termination date | Apr 5, 2017 |
| City | Telford |
| State | PA |
| Country | United States |
| FEI number | 2517967 |
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: