Cobas Infinity Central Lab (2019-06-06)

Starting date:

June 6, 2019

Posting date:

July 5, 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-70357

Last updated: 2019-07-05

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  Reason
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  Affected products

Affected Products

Cobas Infinity Central Lab

Reason

Culture medium identification can be duplicated if the user edits the culture medium identification and deletes or adds culture medium following specific steps.

Affected products