Draeger Globe-Trotter and Globe-Trotter IC — Class II medical device recall Z-1365-2022
Ongoing recall by Draeger Medical Systems, Inc., reported 2022-07-20. The firm has initiated this recall to replace component on devices distributed containing a component within t
| Recall number | Z-1365-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Draeger Medical Systems, Inc., Telford, PA, United States |
| Recall initiated | 2022-05-20 |
| Classified | 2022-07-11 |
| Reported by FDA | 2022-07-20 |
| Quantity | 38 ous |
| Serial numbers | MS20508 |
| Model numbers | MS20508, MS20509 |
Product
Draeger Globe-Trotter and Globe-Trotter IC, Model numbers MS20508 and MS20509. neonatal transport system
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1365-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.