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Heartstart XL+ (2014-03-31)
- Starting date:
- March 31, 2014
- Posting date:
- April 30, 2014
- 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-39217
Recalled pProducts
- Heartstart XL+
Reason
Philips has become aware that a software communication failure on the Heartstart XL+ that occurs during an automated ready-for-use (RFU) test or at turn-on may lock the user out of clinical mode, which may delay therapy.
Affected products
A. Heartstart XL+
Lot or serial number
All lots
Model or catalog number
- 861290
Companies
- Manufacturer
-
Philips Medical Systems
3000 Minuteman Road
Andover
01810
Massachusetts
UNITED STATES