Devices

Device Recall Fujufilm

Model / Serial
Verson 2.2.1 and 2.3.1.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Foreign: Canada, Germany, Israel, Japan
Product Description
Synapse Version 2.2.1 and 2.3.1 software
Manufacturer
Fujifilm Medical System USA, Inc.
1 Event
- Recall of Device Recall Fujufilm

Manufacturer

Fujifilm Medical System USA, Inc.

Manufacturer Address
Fujifilm Medical System USA, Inc., 419 West Avenue, Stamford CT 06902
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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