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Recall Observatory FDA recall evidence

Device product

Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452

Z-2282-2019

February 20, 2019

Class II

Product summary

Firm
Luminex Corporation
Event
Event 83470
Status
Ongoing
Classification
Class II
Quantity
N/A
Official record key
device-enforcement:Z-2282-2019

Official wording

Reason: Through internal investigation, it was discovered that a portion of side cassette assemblies (SCAs) back side seal (BSS) did not meet design specification, resulting in partially sealed SCAs. The impact of a partial seal of the BSS could result in potential decrease of volume for each solution in the SCAs and decreased sensitivity or stability of the assay.

Code information: Lot numbers and discontinue use by date for Part Number 50-10037: AA7125 - Immediately, AA7310 - Immediately, AA7548 - 3/13/2019, AA7633 - 4/12/2019

Distribution pattern: US: AK, AL, AZ,CA,CO,FL,GA,IL,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,NE,NJ,NM,NY,OH,ON,OR,PA,TN,TX,UT,VA,VT,WA,WI, OUS: Belgium, Canada, Thailand, Germany, Singapore, United Kingdom

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Through internal investigation, it was discovered that a portion of side cassette assemblies (SCAs) back side seal (BSS) did not meet design specification, resulting in partially sealed SCAs. The impact of a partial seal of the BSS could result in potential decrease of volume for each solution in the SCAs and decreased sensitivity or stability of the assay.