Miseqdx Cystic Fibrosis 139-variant Assay

Miseqdx Cystic Fibrosis 139-Variant Assay Recall The Miseqdx Cystic Fibrosis 139-Variant Assay, a medical device used to test for cystic fibrosis variants, has been recalled across Canada. The recall was issued due to issues with the device itself. This affects anyone in Canada who may have received or could receive testing with this assay.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-07-07
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/410a29d4-86eb-48b0-a5f1-0252a48f8b19