LifePak15 Monitor/Defibrillator (2020-01-01)
- Starting date:
- January 1, 2020
- Posting date:
- January 20, 2020
- 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-72135
Last updated: 2020-01-21
Affected Products
LifePak15 Monitor/Defibrillator
Reason
During a review of product complaints reviewed from product launch to September 2019, Stryker - Physio Control has become aware that certain LifePak 15 Monitor/Defibrillators may not deliver a defibrillation shock when the device "shock" button is pressed as a result of oxidation that has formed over time within the button. The hard paddle shock button is not affected by this issue.
Affected products
LifePak15 Monitor/Defibrillator
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
More than 10 numbers, contact manufacturer.
Companies
- Manufacturer
-
Physio-Control, Inc.
11811 Willows Road North East
Redmond
98052
Washington
UNITED STATES