Reported Aug 14, 2024 · Ongoing

Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model…

Siemens Medical Solutions USA, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Siemens Medical Solutions USA, Inc · 40 Liberty Blvd · Malvern, PA · 19355-1418

Is this the product you have?

  • Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image
  • Model Number10762471
Lot codes and dates
  • UDISerial
  • NumbersSerial Number
    • 8320
    • 8198
    • 8334
    • 8474
    • 8183
    • 8322
    • 8613
    • 8244
    • 8660
    • 8436
    • 8095
    • 8371
    • 8378
    • 7805
    • 5664
    • 5615
    • 8150
    • 8130
    • 8300
    • 8093
    • 8468
    • 7791
    • 8479
    • 7136
Amount recalled
24 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.