Siemens recalls Luminos dRF Max displays with specific serial numbers due to risk of injury from support arm unintentionally lowering when positioned near people.
The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
Siemens is recalling Luminos dRF Max medical imaging displays with certain serial numbers because the support arm can lower unexpectedly while suspended, potentially causing injury to people nearby. This recall affects medical facilities using these displays.
The support arm of the display can unintentionally lower when suspended near the ceiling or wall. This movement could cause injury to people standing or moving under the display during positioning. The hazard occurs when the display is positioned in a way that people are close to the support arm.
Medical facilities using the Luminos dRF Max displays with specific serial numbers are most at risk. Patients and staff near the display during positioning could be injured if the support arm lowers unexpectedly.
Check the serial number on the display. The affected models have specific serial numbers listed in the recall notice: 8320 8198 8334 8474 8183 8322 8613 8244 8660 8436 8095 8371 8378 7805 5664 5615 8150 8130 8300 8093 8468 7791 8479 7136.
Look for the serial number on the display to confirm if it is one of the affected numbers listed in the recall.
The support arm can unintentionally lower when suspended near the ceiling or wall, potentially causing injury to people nearby during positioning.
Check the serial number on the display. The affected models have specific serial numbers listed in the recall notice: 8320 8198 8334 8474 8183 8322 8613 8244 8660 8436 8095 8371 8378 7805 5664 5615 8150 8130 8300 8093 8468 7791 8479 7136.
The recall does not require immediate stop use; however, you should check the serial number to confirm if your display is affected.
We’ve drafted a message you can send Siemens Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2526-2024 — Siemens Medical Siemens Medical Hello, I own a Siemens Medical that is covered by recall Z-2526-2024 from Siemens Medical. 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.
