Drugs & medicalClass II

Siemens Medical Solutions USA, Inc recalls Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor- 10094135 Artis zee ceiling- 10094137…

Coolant level in the cooling circuit drops below a certain level, this may result in a situation in which the X-ray tube is no longer sufficiently cooled and the system will display the message TUBE HOT, have a break .…

Read the official notice →
Date
2024-04-24
Country
United States
Brand
Siemens Medical Solutions
Product
Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor- 10094135 Artis zee ceiling- 10094137 Artis zee…
Classification
Class II
Units
US 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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2024-07-31
  2. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Sensis Vibe systems with software version VD15B in combination with Sensis High End Server -Intended to be used as a…

    If the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual), the possibility exists that the application…

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide distribution in the states of CA, CT, FL, IA, KS, MA, MI, NJ,…Official notice →
  3. 2024-07-03
  4. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls AXIOM Vertix MD - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as…

    Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide distribution.Official notice →
  5. 2024-05-01
  6. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc. recalls ACUSON Redwood 1.0 Diagnostic Ultrasound System, REF: 11503314, running software version VA10A to VA10G

    On ultrasound systems, when Cardiac DICOM SR feature is configured to display either minimum or maximum measured value, and multiple cardiac region measurements are made, and results are exported into the SR feature,…

    FDA · DeviceSiemens Medical Solutions USA, Inc.Worldwide distribution - US Nationwide including in the states of AL, AR, CA,…Official notice →
  7. 2024-01-17
  8. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Sensis Vibe Hemo

    The possibility of the Sensis documentation functionality application to crash.

    FDA · DeviceSiemens Medical Solutions USA, IncDomestic: CA, CT, & FL.Official notice →
  9. 2023-12-20
  10. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100

    Potential hardware issue for ARTIS icono ceiling system: collision sensor may falsely signal non-existing collisions for up to half an hour when the system is switched off for a longer time (e.g., overnight) and…

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide - Worldwide Distribution: Domestic distribution to FL GA IA IL…Official notice →
  11. 2023-11-22
  12. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Mobilett Mira wireless (VA20) mobile x-ray system(s)

    Due to the incorrect mounting of the buzzer component, there is no acoustic signal during x ray activation. Otherwise, the system is fully functional, and x ray is applied correctly. By means of the additional visual…

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide - WorldwideOfficial notice →
All 70 Siemens Medical Solutions recalls →

Other drugs & medical recalls in the United States

  1. 2024-05-01
  2. US
  3. US
    Drugs & medicalClass I

    Aruba Aloe Balm N.V. recalls Alcoholada Gel, Pain Relieving Gel, 0.5% Lidocaine Hydrochloride, packaged in (a) 8.5 fl oz (251 mL) plastic bottle UPC 0 82252 03120 9…

    Chemical Contamination: Product manufactured with ethanol API that contains methanol

    FDA · DrugAruba Aloe Balm N.V.Nationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass I

    Pyramids Wholesale Inc. recalls Weiner Boner Honey, 12g packet, 100% Organic Formula.

    Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.

    FDA · DrugPyramids Wholesale Inc.Nationwide in the USAOfficial notice →
  5. 2024-04-24
  6. US
    Drugs & medicalClass II

    Smith & Nephew Medical, Ltd. recalls RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who would benefit from a suction pump (NPWT), as it may promote…

    Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump

    FDA · DeviceSmith & Nephew Medical, Ltd.Worldwide distribution - US Nationwide and the countries of Canada, Chile.Official notice →
  7. US
    Drugs & medicalClass II

    Raye's Inc. recalls SW Bari Lift & Transfer, Model Number 38060000

    Retrospective engineering analysis against current ISO standards for hoists has determined: 1. The device cannot physically perform at maximum documented weight specifications when a factor of safety of two times the…

    FDA · DeviceRaye's Inc.Worldwide distribution - US Nationwide and the countries of Australia, UK.Official notice →
  8. US
    Drugs & medicalClass II

    Randox Laboratories Ltd. recalls Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the Microalbumin Assay Catalog Number: MA1567

    Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative bias compared to other methods and may misclassify patient results. Users may experience a shift in Quality Control and patient sample…

    FDA · DeviceRandox Laboratories Ltd.US Nationwide distribution in the states of GA, MA, WV including PR.Official notice →
See all drugs & medical recalls →