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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

GE Healthcare, LLC: The patient monitors may simultaneously restart as designed if all are connected to the same network and a network overload occurs for a prolonged time.

Agency Publication Date: November 29, 2018
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Affected Products

Product: Dash 3000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.

All monitors

Product: Dash 4000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.

All monitors

Product: Dash 5000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.

All monitors

Product: Solar 8000i Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.

All monitors

Product: Solar 8000M Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.

All monitors

Product: Solar 9500 Information Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.

All monitors

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 81058
Status: Active
Manufacturer: GE Healthcare, LLC
Manufactured In: United States
Units Affected: 6 products (Approximately 182,640 monitoring systems for Dash 3000/4000/5000; Approximately 182,640 monitoring systems for Dash 3000/4000/5000; Approximately 182,640 monitoring systems for Dash 3000/4000/5000; Approximately 73,673 Solar 8000i and 8000M monitoring systems; Approximately 73,673 Solar 8000i and 8000M monitoring systems; Approximately 3,864 monitoring systems)

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.