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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

Beckman Coulter Inc.: A defect in the SATA power adapter cable within the instruments computer has the potential risk for an electrical short that may lead to the following outcomes: charring and/or melting of the SATA adapter cable within the computers metal enclosure, smoke emanating from PC6, flames contained within PC6, or an inability to use the devices CD-ROM. ; A defect in the SATA power adapter cable within the instrument s computer has the potential risk for an electrical short that ma

Agency Publication Date: May 9, 2020
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Affected Products

Product: iChem¿VELOCITY Urine Chemistry System-

Catalog #700-7176-001 and #700-7177-001, All part numbers

Product: iQ200 Series Urine Microscopy Analyzer- All part numbers

Catalog Numbers: 00-3322, 700-3325, 700-3326, 700-3345, 700-3347, 700-3370, 700-3375, 700-3300RFB, B48999, C10683, C10684., All part numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85423
Status: Resolved
Manufacturer: Beckman Coulter Inc.
Manufactured In: United States
Units Affected: 2 products (1557 units; 3576 units)
Agency Last Updated: October 26, 2020

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.