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DEFIBRILLATION PADS (2016-01-27)
- Starting date:
- January 27, 2016
- Posting date:
- February 22, 2016
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-57202
Affected Products
DEFIBRILLATION PADS
Reason
Cardiac Science has determined that the affected lot may exhibit higher than expected electrical impedance over time. If electrode impedance becomes too high, the G3 AED will fail the electrode self-test performed by the AED and it will not be rescue ready.
Affected products
DEFIBRILLATION PADS
Lot or serial number
141125-02
Model or catalog number
9131
Companies
- Manufacturer
-
Cardiac Science Corporation
N7W22025 JOHNSON DRIVE
WAUKESHA
53186
Wisconsin
UNITED STATES