Draeger Globe Trotter IC, Catalog Number: MU20509, Draeger… recallZ-1053-2008 · Draeger Medical, Inc. · initiated Jan 31, 2008
Terminated All recalls posted in March 2008
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Draeger Medical, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Heating failure- The power board which controls the incubator heater may not regulate the temperature properly resulting in a high temperature alarm and a loss of temperature control within the patient compartment.
FDA root cause category: Nonconforming Material/Component
What the company is doing
The firm notified consignees on 2/1/08, by an Important Safety Notice. The letter instructed users to remove any units from use until a Draeger Service Representative can replace the power board. A Service Representative will be in contact to schedule a service visit. For questions concerning this recall please contact 215-660-2418 or [email protected].
Recall details
- Recall number
- Z-1053-2008
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Jan 31, 2008
- Posted by the FDA
- Mar 18, 2008
- Recalling firm
- Draeger Medical, Inc.
- Quantity
- 4 units
- Product code
- FMZ
- FDA submissions
- K001019
- Distribution
- Worldwide Distribution-- USA including states MO, OH, and PR, and countries of Australia, Canada, Columbia, Israel, UAE, France, China, Italy, Denmark, Switzerland, and UK.
Product description
Draeger Globe Trotter IC, Catalog Number: MU20509, Draeger Medical, Inc., Telford, PA 18969
Code information (models, lots, serial numbers)
Serial Numbers: QT05675, QT05676, ST05708, and ST05704
Other devices under the same FDA submission
1 device cleared under K001019 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- TI500 Globetrotter Neonatal Transport System MU20508Draeger Medical Systems, Inc. · Incubator, Neonatal Transport1 report
Other products in the same recall event
The FDA groups related products into one recall event (event 46742).
- Z-1052-2008 · TerminatedDraeger GT500. GlobeTrotter Transport System. Catalog Number: MU20508, Draeger Medical, Inc., Telford, PA 18969
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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