Devices

Device Recall S/5 Aneshesia Delivery Unit

Model / Serial
6025108 thru 6025111, 6025114 thru 6025117, 6025119, 6025120, 6025122 thru 6025128, 6025130 thru 6025132, 6025134, 6025136, 6025137, 6035737, 6035738, 6035740 thru 6035745, 6035747, 6035751, 6035757, 6035758, 6035760, 6035762, 6035765, 6035772 thru 6035774, 6035784, 6048756 thru 6048761, 6048764, 6048847, 6048849, 6048853 thru 6048856 and 40300736
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide---USA-States of AZ, CA, IA, MI, TX, and WI ----International- Australia, Austria, Belgium, Finland, Germany, Israel, Italy, Jordan, Malaysia, Netherlands, Norway, Portugal, Slovakia, South Africa, and Turkey.
Product Description
Datex-Ohmeda S/5 Anesthesia Delivery Unit (ADU)
Manufacturer
GE Healthcare
1 Event
- Recall of Device Recall S/5 Aneshesia Delivery Unit

Manufacturer

GE Healthcare

Manufacturer Address
GE Healthcare, 3030 Ohmeda Drive, PO Box 7550, zip 53707-7550, Madison WI 53718
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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