Philips recalls CombiDiagnost R90 1.1 (709031) models where RF viewer may display previous patient radiography images during fluoroscopy, causing image differences. Affected units have specific serial numbers.
While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.
Philips is recalling CombiDiagnost R90 1.1 (709031) models where the RF viewer might show previous patient radiography images during fluoroscopy exams. This could cause differences in image content, format, and size. While not dangerous, it may lead to confusion in medical imaging.
During fluoroscopy exams, the RF viewer may display images from previous patients instead of the current patient. This causes differences in image content, format, and size, potentially leading to confusion in medical imaging.
Healthcare facilities using the CombiDiagnost R90 1.1 (709031) model with specific serial numbers. Medical staff performing fluoroscopy exams are most at risk of image confusion.
Check if your CombiDiagnost R90 1.1 (709031) has serial numbers listed in the recall (e.g., 10001004 to 10001152). The software version is 1.1.1 or higher.
Verify your CombiDiagnost R90 1.1 (709031) has a serial number from the list provided in the recall.
No, this recall involves a potential display of previous patient images during exams, which may cause image differences but does not pose a safety risk.
Check if your CombiDiagnost R90 1.1 (709031) has a serial number listed in the recall (e.g., 10001004 to 10001152). The software version must be 1.1.1 or higher.
The recall does not require immediate action. Affected units may be monitored for image differences during use.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1088-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1088-2024 from Philips. 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.
