Drugs & medicalClass II

GE Healthcare, LLC recalls GE Centricity Universal Viewer Zero Footprint Client

There is a potential to display incomplete patient imaging study.

Read the official notice →
Date
2021-12-08
Country
United States
Brand
GE Healthcare
Product
GE Centricity Universal Viewer Zero Footprint Client
Classification
Class II
Units
Worldwide distribution - US Nationwide distribution in the states of AR, AZ,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 GE Healthcare recalls

  1. 2022-03-23
  2. US
    Drugs & medicalClass II

    GE Healthcare, LLC recalls GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated), REF 2082278-001, and MAS700 (Desktop, REF 2082279-001.

    If the CARESCAPE Central Station v2.0 is used with an unapproved keyboard, the audio can be muted resulting in loss of audible alarms.

    FDA · DeviceGE Healthcare, LLCWorldwide distribution - US nationwide, including Puerto Rico. There was also…Official notice →
  3. 2022-02-16
  4. US
    Drugs & medicalClass II

    GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Artist system, nuclear magnetic resonance imaging system.

    The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.

    FDA · DeviceGE Healthcare, LLCDistribution was nationwide, including Puerto Rico and the Virgin Islands.…Official notice →
  5. 2022-02-02
  6. US
    Drugs & medicalClass II

    GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Sector DICOM"

    The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.

    FDA · DeviceGE Healthcare, LLCDomestic: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY,…Official notice →
  7. 2021-12-01
  8. US
    Drugs & medicalClass II

    GE Healthcare, LLC recalls Computed Tomography Systems Revolution CT, Revolution CT ES, Revolution Apex, Revolution CT with Apex edition

    The accumulated dose is incorrectly displayed in certain situations. Thisoccurs during an interventional exam using the SmartStep option if the table height is adjusted after the exam starts. In this situation, the…

    FDA · DeviceGE Healthcare, LLCWorldwide and US Nationwide DistributionOfficial notice →
  9. 2021-10-27
  10. US
    Drugs & medicalClass II

    GE Healthcare, LLC recalls SIGNA Pioneer nuclear magnetic resonance imaging system

    Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.

    FDA · DeviceGE Healthcare, LLCDistribution in United States to AZ, CA, FL, GA, IL, LA, MA, MD, MN, NC, NH,…Official notice →
  11. 2021-10-13
  12. US
    Drugs & medicalClass II

    GE Healthcare, LLC recalls Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system

    A software anomaly exists in the Centricity Universal Viewer study management feature in which study changes are not propagated to either the Centricity Enterprise Archive (EA) or another Vendor Neutral Archive (VNA).

    FDA · DeviceGE Healthcare, LLCAR, IL, ME, MS, NE, NJ, NY, and TN Belgium, Canada, Costa Rica, France,…Official notice →
All 41 GE Healthcare recalls →

Other drugs & medical recalls in the United States

  1. 2021-12-15
  2. US
  3. US
    Drugs & medicalClass I

    American Screening LLC recalls AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA Vitamin E & Moisturizer, 8 FL OZ (237 mL) bottle with either a…

    Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

    FDA · DrugAmerican Screening LLCDistributed Nationwide in the USAOfficial notice →
  4. 2021-12-08
  5. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting,…

    Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five Dimension Vista Assays

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide distribution and the countries of DE,…Official notice →
  6. US
    Drugs & medicalClass II

    Randox Laboratories Ltd. recalls RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and serum REF: CH200

    When calibrating using the standard provided in the kit, the change in absorbance is lower than expected generating internal quality control results high outside range

    FDA · DeviceRandox Laboratories Ltd.US Nationwide distribution in the states of GA, OR, PA ,WA, West Virginia.Official notice →
  7. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN:…

    Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

    FDA · DeviceBoston Scientific CorporationUS Nationwide distribution.Official notice →
  8. US
    Drugs & medicalClass II

    NuVasive Specialized Orthopedics, Inc. recalls NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product Description:…

    The Instructions for Use have been updated to include: (1) Clarification that the device is intended for use only in patients 18 years and older, (2) That patients should weigh 50 lbs. or more while undergoing…

    FDA · DeviceNuVasive Specialized Orthopedics, Inc.U.S.: AK, AL, AR, AZ, CA, CO, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA,…Official notice →
See all drugs & medical recalls →