Reported Aug 12, 2020 · Terminated

SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage: is a device intended to visualize anatomical…

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

Is this the product you have?

  • SIEMENS
  • Healthineers Uroskop Omnia max Model10762473 -
  • Product Usageis a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image
Lot codes and dates
  • Serial Numbers

    193 of 193 codes

    • 4557
    • 4574
    • 4571
    • 4099
    • 4074
    • 4014
    • 4627
    • 4626
    • 4578
    • 4645
    • 4316
    • 4615
    • 4056
    • 4587
    • 4049
    • 4068
    • 4305
    • 4015
    • 4543
    • 4616
    • 4553
    • 4333
    • 4063
    • 4655
    • 4556
    • 4022
    • 4521
    • 4121
    • 4325
    • 4111
    • 4510
    • 4565
    • 4322
    • 4554
    • 4301
    • 4597
    • 4509
    • 4661
    • 4036
    • 4519
    • 4520
    • 4043
    • 4024
    • 4560
    • 4629
    • 4530
    • 4646
    • 4318
    • 4618
    • 4575
    • 4304
    • 4142
    • 4300
    • 4095
    • 4146
    • 4649
    • 4059
    • 4562
    • 4501
    • 4309
Amount recalled
194 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

Two software issues (1) Using the override function in case of blocked system movements affecting Luminos dRF Max, Luminos Agile Max and Uroskop Omnia Max systems may cause collision of the system under operator control with obstacles or persons .(2) Incorrectly assigned image affecting Ysio Max, Luminos dRF Max and Luminos Agile Max systems with detector MAX Static causing incorrect base for diagnosis

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

Notice updated Jun 21, 2022 · Data as of Sep 19, 7:34 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.