Devices

Device Recall Hitachi AIRIS II Magnetic Resonance Imaging Device

Model / Serial
C002 thru C795, C907, and C910.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
The product was distributed throughout the United States and to one consignee located in both Wales and London.
Product Description
Hitachi AIRIS II Magnetic Resonance Imaging Device
Manufacturer
Hitachi Medical Systems America Inc
1 Event
- Recall of Device Recall Hitachi AIRIS II Magnetic Resonance Imaging Device

Manufacturer

Hitachi Medical Systems America Inc

Manufacturer Address
Hitachi Medical Systems America Inc, 1959 Summit Commerce Park, Twinsburg OH 44087-2371
Manufacturer Parent Company (2017)
Hitachi Ltd
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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