Drugs & medicalClass II

Siemens Medical Solutions USA, Inc recalls ARTIS pheno, Interventional fluoroscopic x-ray system, Model No. 10849000

Siemens has become aware of three potential software issues with ARTIS pheno systems with software version VE10B. This may lead to a hazardous situation for patients if treatment cannot be continued on the system and…

Read the official notice →
Date
2022-11-02
Country
United States
Brand
Siemens Medical Solutions
Product
ARTIS pheno, Interventional fluoroscopic x-ray system, Model No. 10849000
Classification
Class II
Units
Domestic distribution nationwide. Foreign distribution worldwide.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2023-01-25
  2. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor

    Mechanical connection between the tabletop and table base may be lost.

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide distribution - US Nationwide and the countries of Armenia,…Official notice →
  3. 2023-01-11
  4. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Programmable Diagnostic Computer

    The firm will be performing a software update to address a software error which affects the listed products. This correction addresses four potential software issues: 1) "PASSWORD STORE CORRUPTED" error message during…

    FDA · DeviceSiemens Medical Solutions USA, IncDomestic distribution nationwide. Worldwide foreign distribution to Albania…Official notice →
  5. 2022-12-21
  6. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls ARTISTE, ONCOR and PRIMUS with syngo RT Therapist with software version 4.3.1 MR3. Material Number: 8162815 Intended Use:…

    When selecting the site fraction group for treatment, the User may select the wrong site for treatment, and potentially deliver the dose to wrong isocenter

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide distribution in the states of CA, IA, LA, NE, NV, OH, SC.Official notice →
  7. 2022-09-07
  8. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700

    Siemens has become aware of a potential hardware issue with Artis Q, Artis Q.zen, Artis pheno and Artis icono systems with a specific lot of X-ray tubes. In rare cases, if the error detection mechanism fails, it will…

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide Distribution: US (nationwide) and OUS (Foreign) to countries of:…Official notice →
  9. 2022-08-24
  10. US
    Drugs & medicalClass III

    Siemens Medical Solutions USA, Inc recalls AXIOM Sensis or Sensis Vibe Combo systems as follows: System Material # AXIOM Sensis, Combo 64 6623974; AXIOM Sensis, Hemo…

    The Sensis Signal Input Box provides hooks as a milled item on the bottom of the box support the possibility of mounting the Signal Input Box on an accessory rail (e.g., at the patient table), In the event the mounting…

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide Distribution Foreign: Albania Algeria Angola Argentina Armenia…Official notice →
  11. 2022-07-27
  12. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Sensis with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or…

    Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of its communication during the first patient examination of the day or after a longer period of inactivity to the Sensis Vibe system resulting…

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide Distribution AZ FL KY MI OH PR TXOfficial notice →
All 70 Siemens Medical Solutions recalls →

Other drugs & medical recalls in the United States

  1. 2022-11-02
  2. US
    Drugs & medicalClass II

    ConvaTec, Inc recalls ConvaTec Active Life, One-Piece Drainable Pouch, 3/4-2 1/2 in., 19-64mm, REF 400598. For the management of stoma output following a…

    impaired functionality of the release liner

    FDA · DeviceConvaTec, IncUS Nationwide distribution.Official notice →
  3. US
    Drugs & medicalClass II

    Encore Medical, LP recalls EMPOWR Acetabular System, Liner, 10 deg Hooded, HXe+ 40H, REF: 942-01-40H. Orthopedic implant component.

    Hip liner implant boxes may contain knee inserts and knee insert boxes may contain hip liner implants, which may lead to implants not being available for surgeries, which may cause delays in surgery.

    FDA · DeviceEncore Medical, LPUS Nationwide distribution in the states of FL, IN, IL, KY, AZ, TX.Official notice →
  4. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ADLT BLOOD CLUTURE COLLECT KIT, Reorder #: DYNDH1245

    Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an…

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of California.Official notice →
  5. US
    Drugs & medicalClass II

    ZOLL Circulation, Inc. recalls AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR

    Due to increase in Li-Ion Battery failures

    FDA · DeviceZOLL Circulation, Inc.U.S.: AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA,…Official notice →
  6. US
    Drugs & medicalClass I

    Exela Pharma Sciences LLC recalls 8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx only,…

    Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration

    FDA · DrugExela Pharma Sciences LLCNationwide within the United StatesOfficial notice →
  7. US
    Drugs & medicalClass II

    Aurobindo Pharma USA Inc. recalls Quinapril and Hydrochlorothiazide Tablets, USP 20mg/12.5mg, 90 Tablets bottles Distributed by: Aurobindo Pharma USA, Inc. 279…

    CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.

    FDA · DrugAurobindo Pharma USA Inc.NationwideOfficial notice →
See all drugs & medical recalls →