MiSeqDx Cystic Fibrosis 139-Variant Assay (2018-02-13)

Starting date:

February 13, 2018

Posting date:

February 22, 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-66036

• Reason
• Affected products

Affected products

MiSeqDx Cystic Fibrosis 139-Variant Assay

Reason

RMF reagents and other reagents located in the reagent cartridge could potentially be under-filled or empty.

Affected products