Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1489-2021 — VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the reflectometer correction factor adjustment procedure.

U.S. FDA — Device Enforcement · United States · 2021-03-26 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1489-2021
Date of alert
2021-03-26
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ortho-Clinical Diagnostics, INc.
Product category
device
Product type
Devices
Reported risk: Delayed results. Ortho confirmed that two lots of VITROS Black Reference Slides are incorrectly labelled as White Reference Slides. If the customer fails to notice both the product name or the unexpected color of the slides and tries to use Black Reference Slides as White Reference Slides, the Correction Factor test will fail - and the analyzer will not be able to produce results for any assays other than sodium, potassium, and chloride. If the customer doesnt have any White Reference Slides in reserve, they cant run the Correction Factor test correctly and get the analyzer running again until they get more White Reference Slides delivered. This could lead to a delay in results for all Vitros assays except for sodium, potassium, and chloride.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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