GE Healthcare Finland Oy provides a range of medical devices including SWP25100018SA to SWP25090059SA. These products are designed for healthcare applications and are compliant with international standards.
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
GE Healthcare Finland Oy offers medical devices from SWP25100018SA to SWP25090059SA. These products are used in healthcare settings and meet international quality and safety standards.
These products are medical devices designed for healthcare use. They are generally safe when used as intended and comply with international standards. However, improper use or malfunction could pose risks.
Healthcare professionals, medical device users, and patients
Check for proper installation, regular maintenance, and adherence to manufacturer guidelines. Ensure the device is used in a suitable environment and by trained personnel.
Ensure the device is used by trained healthcare professionals.
Follow the manufacturer's instructions for installation and operation.
Perform regular maintenance checks as per the manufacturer's schedule.
These are medical device model numbers from GE Healthcare Finland Oy.
Yes, these devices are designed to be safe when used as intended and comply with international medical device standards.
Yes, it is recommended that healthcare professionals receive proper training before using these devices.
We’ve drafted a message you can send GE Healthcare Finland Oy to request your refund or repair — edit it as you like.
Subject: Recall Z-0456-2026 — GE Healthcare Finland Oy GE Healthcare Finland Oy Hello, I own a GE Healthcare Finland Oy that is covered by recall Z-0456-2026 from GE Healthcare Finland Oy. 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.
