Devices

Device Recall Philips Lumify Diagnostic Ultrasound

Model / Serial
System Serial numbers: USD15L0177; USD15L0178; USD15L0179; USD15L0297; USD15L0298; USN15L0789; USN15L0862; USN15L0863; USN15L0864; USN15L0865; USN15L0866; USN15L0867; USN15L0917; USN15L0918; USN15L0988; USO15L0563; USO15L0564; USO15L0565; USO15L0566; USO15L1087; and USO15L1088.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
distributed in CA, CT, ND, NV, OR, RI, TN, and WA.
Product Description
Philips Lumify Diagnostic Ultrasound, Catalogue Number: 795216 || Part Number: 989605449841 with 453561845331 (software version 1.0)
Manufacturer
Philips Ultrasound, Inc.
1 Event
- Recall of Device Recall Philips Lumify Diagnostic Ultrasound

Manufacturer

Philips Ultrasound, Inc.

Manufacturer Address
Philips Ultrasound, Inc., 22100 Bothell Everett Hwy, Bothell WA 98021-8431
Manufacturer Parent Company (2017)
Philips
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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