Skip to content
Recall Observatory FDA recall evidence

Device product

IMMULITE /IMMULITE 1000 Systems TIE Total IgE, REF LKIE1, SMN 10380867, IVD --- Siemens Healthcare Diagnostics Products Ltd. For in vitro diagnostic use with the IMMULITE, IMMULITE 1000, and IMMULITE 2000/ IMMULITE 2000 XPi Systems Analyzers - for the quantitative measurement of Total Immunoglobulin type E (IgE) in serum.

Z-1517-2014

December 20, 2013

Class II

Product summary

Firm
Siemens Healthcare Diagnostics
Event
Event 67210
Status
Terminated
Classification
Class II
Quantity
5953 units
Official record key
device-enforcement:Z-1517-2014

Official wording

Reason: Siemens confirmed an overall average positive bias of 23% against the WHO 2nd IRP 75/502 with the IMMULITE Systems Total IgE assays.

Code information: Lots 326 through 333

Distribution pattern: Worldwide distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Siemens confirmed an overall average positive bias of 23% against the WHO 2nd IRP 75/502 with the IMMULITE Systems Total IgE assays.