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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

Qiagen Sciences LLC: Increased occurrence rate of false positive results, lead to a false positive sample result that could subsequently be incorrectly reported from the laboratory. A false positive result could lead to the risk of the patient being exposed to an inappropriate or suboptimal anti-cancer treatment and/or unnecessarily experiencing side effects

Agency Publication Date: August 29, 2022
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Affected Products

Product: therascreen FGFR RGQ RT-PCR kit (US IVD) REF 874721

Lot number: 172017274 Exp Date: 10.11.2022 169046366 Exp. Date: 12.06.2022

Lot Numbers:
number
Product: therascreen FGFR RGQ RT-PCR Kit (CE IVD, not sold in the US) REF 874711

Lot number: 172017804 Exp Date: 10.11.2022 169046610 Exp. Date: 12.06.2022

Lot Numbers:
number
Product: FGFR RGQ RT-PCR Kit (RUO, not IVD) REF 8747010

Lot number: 169047135 Exp Date: 12.06.2022 172017806 Exp. Date: 10.11.2022

Lot Numbers:
number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90691
Status: Active
Manufacturer: Qiagen Sciences LLC
Manufactured In: United States
Units Affected: 3 products (22 kits; 29 kits; 9 kits)

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.