Devices

Device Recall Merge LIS software

Model / Serial
Versions: 4.0.1 and earlier.
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
1
Implanted device?
No
Distribution
Distribution was made nationwide and to the Virgin Islands. Foreign distribution was made to the Bahamas.
Product Description
Merge LIS software.
Manufacturer
Merge Healthcare, Inc.
1 Event
- Recall of Device Recall Merge LIS software

Manufacturer

Merge Healthcare, Inc.

Manufacturer Address
Merge Healthcare, Inc., 900 Walnut Ridge Dr, Hartland WI 53029-8347
Manufacturer Parent Company (2017)
International Business Machines Corp.
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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