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McKesson Cardiology Hemo(2014-06-25)
- Starting date:
- June 25, 2014
- Posting date:
- August 25, 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-41197
Recalled Products
McKesson Cardiology Hemo
Reason
Annual maintenance testing for the McKesson Cardiology Hemodynamic front-end parameter boxes: pb1000 & pb2000. McKesson Cardiology Hemo front-end boxes must undergo annual maintenance testing to establish the proper functioning of the parameter boxes, and to identify in a timely manner whether a parameter box is out of calibration.
Affected products
McKesson Cardiology Hemo
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
More than 10 numbers, contact manufacturer.
Companies
- Manufacturer
-
Mckesson Medical Imaging Company
130 - 10711 Cambie Road
Richmond
V6X 3G5
British Columbia
CANADA