Skip to content
Recall Observatory FDA recall evidence

Device product

ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295

Z-2283-2019

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-2283-2019

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 & discontinue use by dates for Part Number 50-10017: AA7308 - Immediately; AA7485 - 2/23/2019; AA7545 - 3/13/2019; AA7625 - 4/10/2019; AA7630 - 3/16/2019; AA7636 - 4/3/2019; AA7945 - 4/25/2019; AA7985 - 5/8/2019

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.

Field note

Send feedback

We'll only use this to respond to your feedback.