Cobas MPX (2017-12-21)

Starting date:

December 21, 2017

Posting date:

January 29, 2018

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-65726

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  Reason
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  Affected products

Affected products

Cobas MPX

Reason

An increased rate of initial reactive results was observed for specific lot of Cobas MPX. As a consequence, the manufacturer requests that customers discontinue and discard any remaining Cobas MPX of lot number 238061.

Affected products