Getinge recalls Flow-i C30 Anesthesia System model 6677300 due to potential cybersecurity vulnerabilities that could allow remote attacks. Affected units include specific serial numbers and UDI-DI codes.
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 C30 Anesthesia System model 667:7300 because it has a cybersecurity vulnerability that could be exploited to cause system failures or remote attacks. This could lead to unsafe medical conditions if the system is compromised.
The system has a potential cybersecurity vulnerability that could allow attackers to remotely access it. This could lead to denial of service, tampering, or code execution, which might disrupt medical operations or cause unsafe patient conditions.
Healthcare providers using the Flow-i C30 Anesthesia System model 6677300 are likely affected. Medical staff handling anesthesia equipment are at the highest risk due to the critical nature of the system.
Check for the model number 6677300 on the Flow-i C30 Anesthesia System. Affected units have specific serial numbers: 1058, 1060, 1167, 1201, and UDI-DI code 07325710001363.
Verify the model number and serial numbers listed in the recall notice to confirm if your device is affected.
The recall states a potential cybersecurity vulnerability could lead to hazardous situations, but specific patient risks are not detailed in the official notice.
Check for the model number 6677300 and serial numbers 1058, 1060, 1167, or 1201 on your Flow-i C30 Anesthesia System.
The official recall notice does not specify a remedy or action steps for affected devices.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0988-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0988-2024 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.
