Draegar Medical Systems recalls Omega patient monitors due to cybersecurity vulnerabilities that could cause device reboots and loss of functionality. Affected units include all software versions and serial numbers sold to healthcare professionals.
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 all Omega patient monitors because of cybersecurity vulnerabilities that may cause the device to reboot, lose functionality, and/or lose communication with healthcare systems. This could disrupt patient care monitoring in medical settings.
Cybersecurity vulnerabilities in the software could cause the patient monitor to unexpectedly reboot, lose functionality, or disconnect from healthcare systems. This might interrupt critical patient monitoring during medical care.
Healthcare professionals using these patient monitors for patient care are most at risk. The recall affects all units sold to physicians, nurses, and technicians who rely on the devices for medical monitoring.
The Omega patient monitors are used by healthcare professionals. All software versions and all serial numbers are affected, with no specific model or date range mentioned.
Verify if the monitor is rebooting or losing communication with healthcare systems.
Reach out to Draegar Medical Systems for guidance on next steps.
Yes, all software versions and all serial numbers are affected.
Check if the monitor is rebooting or losing communication with healthcare systems, then contact Draegar Medical Systems for guidance.
The recall applies to all software versions and all serial numbers, with no specific model or date range mentioned.
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-0975-2019 — Draegar Medical Systems Draegar Medical Systems Hello, I own a Draegar Medical Systems that is covered by recall Z-0975-2019 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.
