Recalls and alerts more than 4 years old are automatically archived. While this information can still be accessed in the database, it has not been altered or updated since it was archived. Web pages that are archived on the Web are not subject to the Government of Canada Web Standards. As per the Communications Policy of the Government of Canada, you can request alternate formats by contacting us.

Mckesson Cardiology Hemo (2014-08-27)

Starting date:
August 27, 2014
Posting date:
September 11, 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-41337

Recalled Products

Mckesson Cardiology Hemo 

Reason

Incorrect hemoglobin values for hemo calculations.  Mckesson has identified a scenario in which the Mckesson Cardiology Hemo calculation section incorrectly converts the hemoglobin value before it is utilized in the applicable formula calculations.  As a result, the formula output is incorrect.

Affected products

Mckesson Cardiology Hemo 

Lot or serial number

MC13.0 HF3

Model or catalog number

13.0
13.0HF1
13.0HF2
13.0HF3
13.1

Companies
Manufacturer
Mckesson Medical Imaging Company
130 - 10711 Cambie Road
Richmond
V6X 3G5
British Columbia
CANADA