Devices

Device Recall The LIFEPAK CR Plus and LIFEPAK EXPRESS Automated External Defibrillators (AEDs)

Model / Serial
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Worldwide Distribution.
Product Description
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. || Automated external defibrillators.
Manufacturer
Physio Control, Inc.
1 Event
- Recall of Device Recall The LIFEPAK CR Plus and LIFEPAK EXPRESS Automated External Defibrillators (AEDs)

Manufacturer

Physio Control, Inc.

Manufacturer Address
Physio Control, Inc., 11811 Willows Rd Ne, Redmond WA 98052-2003
Manufacturer Parent Company (2017)
Stryker
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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