Devices

Device Recall Intellivue X3

Model / Serial
Model 867030 - All devices shipped from June 2017
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
48 Foreign Accounts
Product Description
IntelliVue X3 Patient Monitor.
Manufacturer
Philips Electronics North America Corporation
1 Event
- Recall of Device Recall Intellivue X3

Manufacturer

Philips Electronics North America Corporation

Manufacturer Address
Philips Electronics North America Corporation, 3000 Minuteman Rd, Andover MA 01810-1032
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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