LIFEPAK 15 Monitor/Defibrillator (2019-01-29)
- Starting date:
- January 29, 2019
- Posting date:
- February 12, 2019
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type I
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-69020
Affected Products
LIFEPAK 15 Monitor/Defibrillator
Reason
Stryker has become aware [via customer complaint] that certain LIFEPAK 15 Monitor/Defibrillators were reported to experience a lock-up condition after a defibrillation shock was delivered. This condition is defined as a blank monitor display with LED lights on, indicating power to the device, but no response in the keypad and device functions. A device in this condition has the potential to delay delivery of therapy, and this delay in therapy has the potential to result in serious injury or death.
Affected products
LIFEPAK 15 Monitor/Defibrillator
Lot or serial number
More than 100 numbers, contact manufacturer.
Model or catalog number
99577-000837
99577-000839
99577-001255
99577-001256
99577-001262
99577-XXXXXX
Companies
- Manufacturer
-
Physio-Control Inc.
11811 Willows Road North East
Redmond, Washington
98052
UNITED STATES