Drug recall
Draeger Globe-Trotter and Globe-Trotter IC, Model numbers MS20508 and MS20509. neonatal transport system
FDA recall event 90423 · Class II · Draeger Medical Systems, Inc.
Key facts
| Event ID | 90423 |
|---|---|
| Recall numbers | Z-1365-2022 |
| Recalling firm | Draeger Medical Systems, Inc. |
| Product type | Devices |
| Products | Draeger Globe-Trotter and Globe-Trotter IC, Model numbers MS20508 and MS20509. neonatal transport system |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The firm has initiated this recall to replace component on devices distributed containing a component within the oxygen supply system that is not rated to the working pressure of the system. |
| Initiation date | May 20, 2022 |
| Report date | Jul 20, 2022 |
| City | Telford |
| State | PA |
| Country | United States |
| FEI number | 2510954 |
At a glance
- 1–9 Products in this recall
- 10–99 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: