FDA recall record

Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay in vitro diagnostic system for recall — FDA Z-0850-2015

Illumina has confirmed a software limitation with MiSeq Reporter software (version 2.2.31) when using the MiSeqDx Cystic Fibrosis Clinical Sequencing…

Class IIIclassification
Z-0850-2015official record ID
Dec 31, 2014report date

Recall record at a glance

Official recordZ-0850-2015
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmIllumina Inc.
Report dateDec 31, 2014
Recall initiation dateNov 6, 2014
Quantity19 units
LocationSan Diego, CA, United States

Official product description

Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay in vitro diagnostic system for use on the Illumina MiSeqDx Platform.

Why the product was recalled

Illumina has confirmed a software limitation with MiSeq Reporter software (version 2.2.31) when using the MiSeqDx Cystic Fibrosis Clinical Sequencing Assay on the MiSeqDx instrument.

Distribution information

US: MD, NY Non-US: France

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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