FDA recall record

Illumina MiSeqDx Universal Kit 1.0, PN 15039608 The Illumina MiSeqDx Universal Kit 1.0 is a recall — FDA Z-0849-2015

It was discovered a software limitation with MiSeq Reporter software (version 2.2.31) when using the MiSeqDx Universal Kit 1.0 on the MiSeqDx instrument.…

Class IIclassification
Z-0849-2015official record ID
Dec 31, 2014report date

Recall record at a glance

Official recordZ-0849-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmIllumina Inc.
Report dateDec 31, 2014
Recall initiation dateNov 13, 2014
Quantity13 units
LocationSan Diego, CA, United States

Official product description

Illumina MiSeqDx Universal Kit 1.0, PN 15039608 The Illumina MiSeqDx Universal Kit 1.0 is a set of reagents and consumables used in the processing of human genomic DNA samples derived from peripheral whole blood, and in the subsequent targeted sequencing of the resulting sample libraries. User-supplied analyte specific reagents are required for the preparation of libraries targeting specific genomic regions of interest. The MiSeqDx Universal Kit 1.0 is intended for use with the MiSeqDx instrument.

Why the product was recalled

It was discovered a software limitation with MiSeq Reporter software (version 2.2.31) when using the MiSeqDx Universal Kit 1.0 on the MiSeqDx instrument. The software cannot report insertions or deletions at specific genomic locations with respect to the primer.

Distribution information

US Distribution to the states of AZ, GA, CA, OH, and VA., and one Internationally to France.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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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