Getinge recalls Flow-i C40 Anesthesia System model 6677400 due to potential cybersecurity vulnerability 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-i C40 Anesthesia System model 6677400 because of a potential cybersecurity vulnerability. This could allow attackers to disrupt the system, tamper with its functions, or execute remote code, potentially causing hazardous situations.
The vulnerability allows unauthorized remote access to the anesthesia system. Attackers could disrupt its operation, alter settings, or run malicious code, which might lead to unsafe patient care conditions.
Healthcare professionals using the Flow-i C40 Anesthesia System model 6677400 are likely affected. Patients and staff at medical facilities using this specific model face the highest risk.
Check for the model number 6677400 on the Flow-i C40 Anesthesia System. The system has specific serial numbers listed in the recall notice: 5204 through 5211 and 7185, 7982, 7983, 8426, 8427, 8428, 8445, 8446.
Identify the model number and serial numbers listed in the recall notice to confirm if your system is affected.
This recall specifically affects the Flow-i C40 Anesthesia System model 6677400 with the listed serial numbers. If your system matches these details, it is affected.
The recall notice does not specify a remedy or action for affected systems. You should check the product details to confirm if your system is affected.
Contact Getinge Usa Sales Inc directly for more information about this recall.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0989-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0989-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
