Devices

Device Recall LIFEPAK EXPRESS

Model / Serial
Part number 3202177-00 through -002 Serial numbers listed above with the CR Plus
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Units were distributed worldwide to public access environments.
Product Description
LIFEPAK EXPRESS defibrillator
Manufacturer
Medtronic Emergency Response Systems, Inc.
1 Event
- Recall of Device Recall LIFEPAK EXPRESS

Manufacturer

Medtronic Emergency Response Systems, Inc.

Manufacturer Address
Medtronic Emergency Response Systems, Inc., 11811 Willows Rd Ne, Redmond WA 98052-2003
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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