Skip to content
Recall Observatory FDA recall evidence

Device product

HYTEC 288 System, Model 74007P, automated immunoanalyzer (EIA) instrument. For in vitro diagnostic use only. HYTEC AUTOSTAT II RF assays: HYTEC AUTOSTAT II RF IgM Kit: Part Number FGA 05, HYTEC AUTOSTAT II RF IgA Kit: Part Number FGA 06, HYTEC AUTOSTAT II RF IgG Kit: Part Number FGA 07, HYTEC AUTOSTAT II Total Rheumatoid Factor Kit: Part Number FGA 08.

Z-2200-2019

March 19, 2018

Class II

Product summary

Firm
Hycor Biomedical Inc
Event
Event 83268
Status
Ongoing
Classification
Class II
Quantity
288
Official record key
device-enforcement:Z-2200-2019

Official wording

Reason: Reports when using Rheumatoid Factor test kits, control and negative samples may be elevated following a sample containing high levels of IgG . The negative control may report out of range; a negative sample may recover as a low positive which could contribute to an incorrect or premature diagnosis of rheumatoid.

Code information: All lots of RF assay

Distribution pattern: Worldwide distribution to US state of TX , Netherlands, Belgium, Austria, Italy, and India

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Reports when using Rheumatoid Factor test kits, control and negative samples may be elevated following a sample containing high levels of IgG . The negative control may report out of range; a negative sample may recover as a low positive which could contribute to an incorrect or premature diagnosis of rheumatoid.

Field note

Send feedback

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