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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