Cobas MPX (2018-04-13)

Starting date:

April 13, 2018

Posting date:

May 1, 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-66634

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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 96 tests. As a consequence, the manufacturer requested that customers discontinue and discard any remaining cobas MPX 96 test of lot 242567.

Affected products