Philips recalls specific MultiDiagnost Eleva models due to hand switch button not fully releasing, which may cause loss of imaging or unintended radiation exposure. Affected models include 708032-708038.
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection
Philips is recalling certain MultiDiagnost Eleva medical imaging devices because a hand switch button may not fully release, leading to loss of imaging or unintended radiation exposure. This could affect medical staff using these devices in hospitals or clinics.
The hand switch button on these devices may not fully release, causing the imaging system to lose functionality or expose patients to unintended radiation. This could happen during routine use, especially if the button is pressed repeatedly or not fully released.
Medical professionals using Philips MultiDiagnost Eleva systems with model numbers 708032 through 708038 are most at risk. Hospitals and clinics that have these specific models should check their equipment.
Check the model number on your Philips MultiDiagnost Eleva device. Affected models include 708032, 708034, 708036, 708037, and 708038. These models were sold with flat detectors or standard configurations.
Identify the model number on your Philips MultiDiagnost Eleva device to confirm if it is affected (708032, 708034, 708036, 708037, or 708038).
Models 708032, 708034, 708036, 708037, and 708038 for Philips MultiDiagnost Eleva with flat detectors or standard configurations.
The hand switch button may not fully release, leading to loss of imaging functionality or unintended radiation exposure.
No. The recall requires checking the model number and taking no immediate action, as the remedy is not specified.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2411-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-2411-2026 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.
