---
title: "Draeger Globe-Trotter and Globe-Trotter IC, Model numbers MS20508 and MS20509... — FDA record Z-1365-2022 | Is It on Recall"
description: "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 w"
url: https://isitonrecall.com/recall/fda-device-z-1365-2022-draeger-globe-trotter-and-globe-trotter-ic-model-numbers-ms20508-and-ms20509-neonatal-transport-syst/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Draeger Globe-Trotter and Globe-Trotter IC, Model numbers MS20508 and MS20509. neonatal transport system — FDA record Z-1365-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 20, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Draeger Globe-Trotter and Globe-Trotter IC, Model numbers MS20508 and MS20509. neonatal transport system
- **Reason**: 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.
- **Classification**: Class II
- **Recalling firm**: Draeger Medical Systems, Inc.
- **Quantity**: 38 OUS (no US distribution)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1365-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1365-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model, country, and serial number: MS20508: El Salvador DSPN-0003 Mexico DSPM-0003, DSPH-0002 Chile DSPL-0003 Saudi Arabia DSPJ-0003, DSPL-0004, DSPL-0005, DSPL-0006, DSPL-0007, DSPM-0001, DSPM-0002, DSPL-0008, DSPK-0002, DSPH-0003, DSPJ-0004, DSRA-0001 Kuwait DSPJ-0002, DSPK-0001 India DSPN-0001, DSPN-0002, DSRA-0002 Taiwan DSPL-0001, SPL-0002, DSPJ-0001 MS20509: Germany DSPH-0003 Qatar DSPL-0007, DSRB-0001 Spain DSPK-0002, DSPJ-0006, DSPJ-0003, DSPH-0001, DSPJ-0004, DSPK-0001, DSPL-0008 Hungary DSPF-0003 Belarus DSPJ-0005 United Kingdom DSPF-0002 Italy DSPJ-0002 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

No US distribution. Foreign distribution to BY, CL, DE, ES, GB, HU, IN, IT, KW, MX, SA, SV, TW.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Delaware](https://isitonrecall.com/state/delaware/)
- [Indiana](https://isitonrecall.com/state/indiana/)

## Dates in the source

- **Report date**: Jul 20, 2022
- **Recall initiation date**: May 20, 2022
- **Center classification date**: Jul 11, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1365-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Draeger Medical Systems, Inc. records](https://isitonrecall.com/brand/draeger-medical-systems-inc/)