Draegar Medical Systems recalls Infinity Delta Series patient monitors due to cybersecurity vulnerabilities that may cause device reboots, loss of function, and communication issues. Affected models include Delta, Delta XL, and Kappa monitors.
The firm is recalling their Delta family of patient monitors software due to cybersecurity vulnerabilities, which may cause the device to reboot, lose functionality, and/or lose communication.
Draegar Medical Systems is recalling their Infinity Delta Series patient monitors (Delta, Delta XL, Kappa models) because of cybersecurity vulnerabilities that could cause the device to reboot, lose functionality, or lose communication with other systems. This risk affects patient monitoring safety in medical settings.
Cybersecurity vulnerabilities in the software could cause the patient monitors to unexpectedly reboot, lose functionality, or disconnect from other medical systems. This may disrupt critical patient monitoring and lead to potential safety risks during medical procedures.
Healthcare providers using the Infinity Delta Series patient monitors for adult, pediatric, or neonatal patients are affected. The risk is highest for medical facilities that rely on these monitors for critical patient monitoring.
Check for the Infinity Delta Series monitors labeled Delta, Delta XL, or Kappa. These monitors are used in medical settings for adult, pediatric, and neonatal patients (excluding specific cardiac and respiratory parameters for neonates).
Verify if the monitor is rebooting, losing functionality, or disconnecting from other systems.
Reach out to Draegar Medical Systems for guidance on next steps and potential software updates.
The Infinity Delta Series monitors (Delta, Delta XL, and Kappa models) are affected.
Your monitor may show unexpected reboots, loss of functionality, or disconnection from other medical systems.
The recall record does not specify a fix or remedy; contact Draegar Medical Systems for guidance.
We’ve drafted a message you can send Draegar Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0974-2019 — Draegar Medical Systems Draegar Medical Systems Hello, I own a Draegar Medical Systems that is covered by recall Z-0974-2019 from Draegar Medical Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
