Device product
VITROS Immunodiagnostic Products - FSH Reagent Pack (10758750000302) 1931922
Z-0059-2019
Product summary
- 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
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.