Getinge recalls Flow-i C20 Anesthesia System model 6677200 due to potential cybersecurity vulnerabilities that could allow remote attacks, leading to system disruption or tampering.
Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.
Getinge is recalling its Flow-i C20 Anesthesia System (model 6677200) because of a cybersecurity vulnerability that could let attackers remotely disrupt or tamper with the system. This could create hazardous situations during medical procedures.
The system has a potential cybersecurity vulnerability that could allow remote attackers to cause a Denial of Service attack, tamper with the device, or execute remote code. This could lead to hazardous situations during medical procedures if the system is compromised.
Healthcare professionals using the Flow-i C20 Anesthesia System model 6677200 are affected. Patients undergoing anesthesia procedures with this device face the highest risk.
Check for the model number 6677200 on the Flow-i C20 Anesthesia System. The device has specific serial numbers listed in the recall notice, including UDI-DI: 07325710001349.
Verify the model number on your Flow-i C20 Anesthesia System to see if it matches the recalled model 6677200.
The recall states a potential cybersecurity vulnerability could lead to hazardous situations, but the exact risk level isn't specified in the notice.
Check for the model number 6677200 on your Flow-i C20 Anesthesia System. The device has specific serial numbers listed in the recall notice, including UDI-DI: 07325710001349.
The recall notice does not specify a remedy, so no action is required beyond checking if your device is affected.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0987-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0987-2024 from Getinge. 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.
