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Vitek MS Plus
- Starting date:
- February 28, 2017
- Posting date:
- April 4, 2017
- 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-62888
Reason
The Vitek MS Plus System could give, in specific conditions, an incorrect identification result if the tested species is not included in the Vitek MS plus knowledge base (KB).
Affected products
Vitek MS Plus
Lot or serial number
version 2.0
version 3.0
Model or catalog number
410895
Companies
- Manufacturer
-
Biomerieux Sa
376 Chemin De L'orme
Marcy-l'etoile
69280
FRANCE