Drugs & medicalClass II

GE Vingmed Ultrasound As recalls GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW

GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner…

Read the official notice →
Date
2024-07-17
Country
United States
Brand
GE Vingmed Ultrasound As
Product
GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
Classification
Class II
Units
US: IL, MA, NM, NY, OK,
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Vingmed Ultrasound As recalls

  1. 2023-07-19
  2. US
    Drugs & medicalClass II

    GE Vingmed Ultrasound As recalls GE Healthcare Vivid S60N, ultrasound device

    GE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If this occurs, it can delay availability of the device in time-critical emergency situations.

    FDA · DeviceGE Vingmed Ultrasound AsWorldwide distribution.Official notice →
All 2 GE Vingmed Ultrasound As recalls →

Other drugs & medical recalls in the United States

  1. 2024-07-17
  2. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150A-1ENB. The Electrocardiograph is one of the tools…

    During manufacturing, the step to install an Electromagnetic Interference (EMI) Absorber was omitted. The purpose of the EMI absorber is to prevent EMI leakage that might potentially affect other devices in the…

    FDA · DeviceBaxter Healthcare CorporationDistribution to Illinois.Official notice →
  3. US
    Drugs & medicalClass II

    SVS LLC recalls Non-sterile, single use, disposable gloves intended for medical purposes to be worn on the hands of examiners to prevent contamination…

    Firm received complaints regarding skin irritation when using the gloves, disintegration of the gloves when used with certain cleaning solutions, and mislabeled products (e.g., outer box indicating one size, but inner…

    FDA · DeviceSVS LLCUS Nationwide distribution in the states of MI, NE, FL, GA, PA, AR, CO, and NY.Official notice →
  4. US
    Drugs & medicalClass II

    Preat Corp recalls 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture…

    Due to incorrect milled titanium abutment being packaged and labeled.

    FDA · DevicePreat CorpU.S.: CA, MO, and NV. O.U.S.: NoneOfficial notice →
  5. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 (Duo Surgical Lights}; b) 4038310 (Trio/Quad Surgical Lights)

    Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and…

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution.Official notice →
  6. US
    Drugs & medicalClass II

    American Contract Systems Inc recalls TOTAL KNEE - 302497- Procedure tray Catalog Number: ANTK12AF

    Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.

    FDA · DeviceAmerican Contract Systems IncUS Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Getinge Usa Sales Inc recalls ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4

    The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational…

    FDA · DeviceGetinge Usa Sales IncDomestic: KY, NC, NY, VA. International: Australia, Bulgaria, Croatia, Czech…Official notice →
See all drugs & medical recalls →