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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Ortho-Clinical Diagnostics: This product is not meeting the current storage labeling for unopened VITROS DAT Performance Verifiers causing customers to obtain lower than expected VITROS BENZ results when using this control.

Agency Publication Date: March 6, 2018
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Affected Products

Product: VITROS Chemistry Products DAT Performance Verifier I in vitro diagnostic

Catalog# 6802327 Lot# H5616

Lot Numbers:
H5616
Product: VITROS Chemistry Products DAT Performance Verifier II in vitro diagnostic

Catalog# 6802328 Lot# J5617

Lot Numbers:
J5617
Product: VITROS Chemistry Products DAT Performance Verifier III in vitro diagnostic

Catalog# 6802329 Lot# K5618

Lot Numbers:
K5618
Product: VITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic

Catalog# 6802330 Lot# L5619

Lot Numbers:
L5619
Product: VITROS Chemistry Products DAT Performance Verifier V in vitro diagnostic

Catalog# 6802331 Lot# M5620

Lot Numbers:
M5620

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79155
Status: Resolved
Manufacturer: Ortho-Clinical Diagnostics
Manufactured In: United States
Units Affected: 5 products (349; 323; 180; 196; 102)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.