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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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF): Vulnerabilities have been identified in the SDN download process that may allow an individual with malicious intent to update the programmers with non-Medtronic software during an SDN download.

Agency Publication Date: November 8, 2018
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Affected Products

Product: Medtronic CareLink 2090 Programmer

All Serial Numbers

Product: Medtronic CareLink Encore 29901 Programmer

All Serial Numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 81300
Status: Active
Manufacturer: Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Manufactured In: United States
Units Affected: 2 products (30172 units; 4072 units)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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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.