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Recall Observatory FDA recall evidence

Device product

Alinity i Ferritin Reagent Kit, List Number 07P6530 The Alinity i Ferritin assay is a chemiluminescent microparticle immunoassay (CMIA) used for the quantitative determination of ferritin in human serum and plasma on the Alinity i analyzer.

Z-2208-2019

November 21, 2018

Class II

Product summary

Firm
Abbott Ireland Diagnostics Division
Event
Event 83341
Status
Terminated
Classification
Class II
Quantity
216 units
Official record key
device-enforcement:Z-2208-2019

Official wording

Reason: Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

Code information: UDI/ Lot Numbers: (01)00380740131487 (17)190730(10)91532UI00/91532UI00, (01)00380740131487 (17)190905(10)93238UI00/93238UI00

Distribution pattern: US Distribution to states of: AR, FL, GA, MD, OK and VA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.