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Recall Observatory FDA recall evidence

Device product

VITROS Immunodiagnostic Products - FSH Reagent Pack (10758750000302) 1931922

Z-0059-2019

July 12, 2018

Class II

Product summary

Firm
Ortho Clinical Diagnostics Inc
Event
Event 80717
Status
Ongoing
Classification
Class II
Quantity
1955
Official record key
device-enforcement:Z-0059-2019

Official wording

Reason: The recalling firm determined that biased results may occur for specific VITROS Immunodiagnostic Products (MicroWell Assays) at biotin concentrations which are lower than indicated in the current Instructions For Use (IFU). Patients who are taking biotin supplements could potentially have biased sample results for affected assays at biotin concentrations lower than indicated in the current IFU.

Code information: 2470 2480 2490 2500 2510 2520 2530

Distribution pattern: Worldwide Distribution - US Nationwide distribution, and countries of Australia, Bermuda, Brazil, Canada, Chile, China, Colombia, India, Japan, Mexico, Singapore, United Kingdom, France, Germany, Italy, Spain, Portugal, Poland, Russia, Denmark, Norway, Sweden, Belgium, and Netherlands.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The recalling firm determined that biased results may occur for specific VITROS Immunodiagnostic Products (MicroWell Assays) at biotin concentrations which are lower than indicated in the current Instructions For Use (IFU). Patients who are taking biotin supplements could potentially have biased sample results for affected assays at biotin concentrations lower than indicated in the current IFU.