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Recall Observatory FDA recall evidence

Device product

VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198

Z-1113-2022

March 25, 2022

Class II

Product summary

Firm
Ortho-Clinical Diagnostics, Inc
Event
Event 90047
Status
Ongoing
Classification
Class II
Quantity
1575 units total: 1183 US; 392 OUS
Official record key
device-enforcement:Z-1113-2022

Official wording

Reason: Falsely high or delayed patient and QC results may occur due to low end imprecision. VITROS Immunodiagnostic Products FSH, LH and Prol Reagents Low End Imprecision. Low-level quality control (QC) and patient samples at the low end of the Measuring (Reportable) Range when using VITROS FSH, LH and Prol Reagent. Calibration failures, driven by imprecision observed with Calibrator Level 1.

Code information: Until further notice, future lots will also be affected. UDI: 10758750008902 Affected Lot Number/ Expiration Date: 1910 14-AUG-2022 1920 19-SEP-2022 1930 19-OCT-2022 1940 31-OCT-2022 1950 28-JAN-2023 1960 31-JAN-2023

Distribution pattern: Worldwide Distribution: US (Nationwide) OUS (Foreign): Australia Bermuda Brazil Canada L3R 4G5 Chile China Colombia Denmark France Germany India Italy Japan Mexico Netherlands Norway Portugal Russia Singapore Spain Sweden United Kingdom

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Falsely high or delayed patient and QC results may occur due to low end imprecision. VITROS Immunodiagnostic Products FSH, LH and Prol Reagents Low End Imprecision. Low-level quality control (QC) and patient samples at the low end of the Measuring (Reportable) Range when using VITROS FSH, LH and Prol Reagent. Calibration failures, driven by imprecision observed with Calibrator Level 1.