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Health product recall

Instrument Manager (2013-12-06)

Starting date:
December 6, 2013
Posting date:
February 3, 2014
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-37559

Recalled Products

Instrument Manager 

Reason

Subsequent child rules may not be evaluated if a rule attempts to divide by zero or another error occurs in a large rule set.  If rules are not evaluated it could produce undesired and/or incorrect results. This could cause harm to the patient if a medical decision is made based upon the erroneous result of the rule processed, or not processed.

Affected products

Instrument Manager

Lot or serial number

V8.12.01
V8.12.02
V8.12.10
V8.12.11
V8.12.20
V8.12.21

Model or catalog number

V8.12.01
V8.12.01
V8.12.02
V8.12.02
V8.12.10
V8.12.10
V8.12.11
V8.12.11
V8.12.20
V8.12.20
V8.12.21
V8.12.21

Companies
Manufacturer
Data Innovations LLC
120 Kimball Ave. Suite 100
South Burlington
05403
Vermont
UNITED STATES