Drugs & medicalClass II

Siemens Medical Solutions USA, Inc recalls UROSKOP Omnia Max. Model Number: 10762473

A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.

Read the official notice →
Date
2025-06-25
Country
United States
Brand
Siemens Medical Solutions
Product
UROSKOP Omnia Max. Model Number: 10762473
Classification
Class II
Units
Nationwide distribution.
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Siemens Medical Solutions recalls

  1. 2025-10-08
  2. US
    Drugs & medicalClass I

    Siemens Medical Solutions USA, Inc recalls MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515,…

    There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a…

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide distribution - US Nationwide and the countries of United Arab…Official notice →
  3. 2025-09-17
  4. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Artis Pheno. Image-Intensified Flouroscopic X-Ray System.

    Limited system movements after startup .

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide distribution in the states of AL, AZ, FL, KY, MA, MI, NY, OR, A,…Official notice →
  5. 2025-07-09
  6. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system

    In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high…

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide.Official notice →
  7. 2025-02-05
  8. US
    Drugs & medicalClass II

    SIEMENS MEDICAL SOLUTIONS USA, INC recalls ARTIS One Angiographic X-Ray System

    A potential issue with ARTIS One systems was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue…

    FDA · DeviceSIEMENS MEDICAL SOLUTIONS USA, INC23 Distributed in the USOfficial notice →
  9. 2024-10-02
  10. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc. recalls ACUSON Juniper 1.0, 1.5, 2.0, 2.5 Diagnostic Ultrasound Systems, REF: 11335791, with software. ACUSON Juniper Select 2.0,…

    If ultrasound systems with software, are changed from factory default to : 1) Milliliters per second (ml/sec, mL/sec) or 2) Milliliters per minute (ml/min, mL/min); then systems will perform incorrect unit conversion…

    FDA · DeviceSiemens Medical Solutions USA, Inc.US: MS, WA, TX, NJ, GA, PN, NY, AL, MN, NE, IN, CT, CA, IL, TN, WI, ND, NM,…Official notice →
  11. 2024-08-14
  12. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls LUMINOS Lotus Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model…

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

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide distribution.Official notice →
All 70 Siemens Medical Solutions recalls →

Other drugs & medical recalls in the United States

  1. 2025-06-25
  2. US
    Drugs & medicalClass II

    BALT USA, LLC recalls Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 00810068567663 PRES1245CPKPLT 00810068567694…

    Due to radiopaque (RO) marker was not visible during angiography and it was determined that the RO marker was not manufactured to specification.

    FDA · DeviceBALT USA, LLCWorldwide - U.S. Nationwide distribution including in the states of AL, AR,…Official notice →
  3. US
    Drugs & medicalClass II

    Preat Corp recalls Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with…

    Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.

    FDA · DevicePreat CorpU.S. Nationwide distribution in the states of AZ, CA, GA, MO, NJ, NY, OH, PA,…Official notice →
  4. US
    Drugs & medicalClass II

    Chamberlain Technologies LLC recalls SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415

    Potential presence of residual adhesive material on the mesh surface.

    FDA · DeviceChamberlain Technologies LLCUS distribution to states of: Illinois, Nebraska, & CaliforniaOfficial notice →
  5. US
    Drugs & medicalClass II

    Ohio Medical Corporation recalls GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S

    Erroneous calibration values, potentially resulting in: as the device ages, oxygen purity will gradually decrease to the point where the device alarms to indicate low oxygen purity will be incorrect.

    FDA · DeviceOhio Medical CorporationUS Nationwide distribution in the states of AR, FL, VA, ND, MS, MN, CA, NV, KY.Official notice →
  6. US
    Drugs & medicalClass II

    Guangzhou Pluslife Biotech Co., Ltd. recalls Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid Testing Card Model/Catalog Number: RM1010202…

    Devices were distributed in the U.S. market without obtaining the required FDA premarket authorization (e.g., 510(k) clearance or PMA).

    FDA · DeviceGuangzhou Pluslife Biotech Co., Ltd.Worldwide distribution: US (nationwide) and OUS (foreign) to countries of:…Official notice →
  7. US
    Drugs & medicalClass II

    Orthofix Srl recalls REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile

    Retrospective; Their is the potential that implantable intramedullary lengthening nails may bend at the distal tail during insertion resulting in having to be replaced.

    FDA · DeviceOrthofix SrlUS: Unknown, OUS: UnknownOfficial notice →
See all drugs & medical recalls →