Getinge recalls Flow-e Anesthesia System model 6887900 due to potential cybersecurity vulnerabilities that could lead to denial of service, tampering, or remote code execution.
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-e Anesthesia System model 6887900 because it has a cybersecurity vulnerability that could allow attackers to disrupt its operation or take control of it remotely. This could lead to hazardous situations during medical procedures.
The system has a potential cybersecurity vulnerability that could allow unauthorized remote access. Attackers might use this to disrupt the system's operation, tamper with its functions, or execute malicious code, which could lead to hazardous situations during medical procedures.
Healthcare providers using the Flow-e Anesthesia System model 6887900 are affected. Medical facilities that have this specific model are at risk of potential cybersecurity issues.
Check for the model number 6887900 on the Flow-e Anesthesia System. The serial numbers listed in the recall include specific numbers starting with 50000.
Identify if your Flow-e Anesthesia System has the model number 6887900 and the listed serial numbers.
The recall states there is a potential cybersecurity vulnerability that could lead to denial of service, tampering, or remote code execution, which might cause hazardous situations. However, the exact risk level isn't specified in the notice.
Check if your Flow-e Anesthesia System has the model number 6887900 and the specific serial numbers listed in the recall (e.g., 50012, 50030, etc.).
The recall does not specify a remedy, so no action is required beyond checking if your system 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-0991-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0991-2024 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.
