Devices

Device Recall Philips Digital Diagnost VE

Model / Serial
Site numbers: 82652, 82681, 82723, 82730, 83073, 85495, 85696, 85697, 85698, 86222, 86382, 86383, 86987, 86988, 100572, 100806, 101933, 102030, 102100, 102115, 102116, 102117, 102489, 102539, 102596, 102713, 102717, 102719, 102787, 102905, 103109, 103165, 103262, 103271, 103272, 103436, 103437, 103438, 103439, 103453, 103511, 103778, 103893, 103894, 103953, 103971, 103976, 104014, 104338, 104465, 104578, 104673, 104676, 104864, 104902, 104903, 104904, 104937, 104938, 105158, 105198, 105199, 105322, 105367, 105415, X1641, X1642, X1650, X1767, X1768. The firm uses site numbers instead of serial numbers.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
The firm distributed to medical facilities nationwide.
Product Description
Digital Diagnost VE
Manufacturer
Philips Medical Systems Sales & Service Region No. America
1 Event
- Recall of Device Recall Philips Digital Diagnost VE

Manufacturer

Philips Medical Systems Sales & Service Region No. America

Manufacturer Address
Philips Medical Systems Sales & Service Region No. America, 22100 Bothell Everett Highway, Bothell WA 98041
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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