Philips recalls CombiDiagnost R90 1.0 (709030) models due to potential display of previous patient radiography images during fluoroscopy exams, causing image content differences.
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 1.0 (709030) models because they may display previous patient radiography images during fluoroscopy exams, leading to differences in image content, format, and size. This could cause confusion in medical imaging procedures.
The device may display previous patient radiography images alongside the current fluoroscopy image during examinations. This causes differences in image content, format, and size, potentially leading to confusion in medical imaging procedures.
Healthcare facilities using the CombiDiagnost R90 1.0 (709030) models with serial numbers listed in the recall notice are most at risk. Patients receiving fluoroscopy exams using these devices may experience image confusion.
Check for the model number R90 1.0 (709030) with serial numbers listed in the recall notice. The software version is 1.1.1 or higher. The device has a unique identifier (UDI DI) of 00884838076747.
Verify your device's serial number against the list of affected units provided in the recall notice.
Philips recalls CombiDiagnost R90 1.0 (709030) models because they may display previous patient radiography images during fluoroscopy exams, causing differences in image content, format, and size.
The official recall notice does not specify a remedy or action steps for affected devices.
Check for the model number R90 1.0 (709030) with serial numbers listed in the recall notice. The software version is 1.1.1 or higher, and the device has a unique identifier (UDI DI) of 00884838076747.
We’ve drafted a message you can send Philips Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1087-2024 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-1087-2024 from Philips Medical Systems. 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.
