Draegar recalls Infinity M300 telemetry monitoring devices with software versions VG2.3.1 and lower due to cybersecurity vulnerabilities including DDoS, spoofing, and tampering risks.
The devices have potential cybersecurity vulnerabilities, which can include Distributed Denial of Service (DDoS), Spoofing, and Tampering.
Draegar is recalling Infinity M300 telemetry monitoring devices with software versions VG2.3.1 and lower because they have cybersecurity vulnerabilities that could allow unauthorized access, data tampering, or denial of service attacks. This affects medical devices used in healthcare settings where security is critical.
The devices have potential cybersecurity vulnerabilities that could allow attackers to send malicious commands, disrupt device operation, or intercept sensitive patient information. These vulnerabilities exist in the software versions listed and could be exploited without user interaction.
Healthcare providers using the Infinity M300 devices with software versions VG2.3.1 and lower are most at risk, as these vulnerabilities could compromise patient data and device functionality.
Check if your Infinity M300 device has software version VG2.3.1 or lower, or model numbers MS25755, MS26076, MS26031, MS18623, or MS22862. The devices were sold to healthcare facilities and may be used in medical settings.
Identify your device's software version by checking the device settings or documentation.
Software versions VG2.3.1 and lower are affected.
Model numbers MS25755, MS26076, MS26031, MS18623, and MS22862 are recalled.
Check if your device has software version VG2.3.1 or lower or one of the model numbers listed in the recall notice.
We’ve drafted a message you can send Draegar to request your refund or repair — edit it as you like.
Subject: Recall Z-0372-2020 — Draegar Draegar Hello, I own a Draegar that is covered by recall Z-0372-2020 from Draegar. 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.
