VITEK MS (2019-04-19)

Starting date:

April 19, 2019

Posting date:

May 17, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-69942

Last updated: 2019-05-17

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  Reason
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  Affected products

Affected Products

VITEK MS

Reason

This issue only concerns the VITEK MS preparation station software when used in conjunction with the VITEK 2 ID/AST cards during test registration in the software.

Based on customer complaints, an error message can be encountered during the VITEK MS / VITEK 2 ID/AST card registration workflow when using the VITEK MS preparation station software to register VITEK 2 ID/AST cards.

Affected products