Drugs & medicalClass II

NovaSignal Corp. recalls NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2

Due to inadvertently disconnecting grounding cable of ultrasound system could result in electrical shock, electrical interference and/or equipment malfunction.

Read the official notice →
Date
2024-07-03
Country
United States
Brand
NovaSignal
Product
NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of MA, TX, NY, MN, 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 Details may be shortened or out of date; the official notice is the authoritative source.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 NovaSignal recalls

  1. 2023-02-08
  2. US
    Drugs & medicalClass II

    NovaSignal Corp. recalls NovaGuide Intelligent Ultrasound System, Model: NA-RBTSYS1. Comprised of NovaBot Automated Headset (AKA: NeuralBot, Model: NA-RBT1) and…

    Transcranial Doppler/ultrasound system tablet has a faulty hard drive, which will cause the system to freeze and reboot. Initially, the system will reboot to a normal operable state but eventually the system will be…

    FDA · DeviceNovaSignal Corp.US Nationwide and Worldwide Distribution: AZ, TX, SC, PA, IL. OUS: CA, SE, NLOfficial notice →
All 2 NovaSignal recalls →

Other drugs & medical recalls in the United States

  1. 2024-07-03
  2. US
    Drugs & medicalClass II

    Centers For Disease Control and Prevention recalls CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11

    The H5b component may fail to amplify, resulting in an inconclusive result.

    FDA · DeviceCenters For Disease Control and PreventionUS Nationwide distribution.Official notice →
  3. US
    Drugs & medicalClass II

    Stryker GmbH recalls Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.

    The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.

    FDA · DeviceStryker GmbHWorldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA,…Official notice →
  4. US
    Drugs & medicalClass II

    Merit Medical Systems, Inc. recalls Prelude Roadster Guide Sheath REF: -PG4F45S -PG4F90S -PG5F45MP -PG5F45R -PG5F45S -PG5F45S018 -PG5F90MP -PG5F90S -PG5F90S018 -PG6F45HS…

    Due to older version of Instruction for Use (IFU) instructing to ensure that the value and the sheath are tightly connected before use. This may cause users to over-tightening the luer which may result in the swivel…

    FDA · DeviceMerit Medical Systems, Inc.Worldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
  5. US
    Drugs & medicalClass II

    Thoratec Switzerland GMBH recalls 2nd Generation CentriMag Primary Console, REF: 201-90401, 201-90701, 201-90411, 201-90421, 201-30300, L201-90401, L201-90411,…

    Due to a component change, the console part of a circulatory support system may not conform to the IEC 61000-4-5 standard, so if subjected to a power surge above 1.8kV and up to 2.0 kV, the console may shut down…

    FDA · DeviceThoratec Switzerland GMBHWorldwide - US Nationwide distribution included in the states of CA, PA, FL,…Official notice →
  6. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics Inc recalls Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Siemens Material Number: 11416751 RAPIDPoint 500e Blood Gas…

    Siemens Healthineers has identified an issue with the RAPIDPoint500e system software version 5.3. This issue affects how the sample source is identified at the LIS when using the capillary mode. With this software…

    FDA · DeviceSiemens Healthcare Diagnostics IncWorldwide - US Nationwide distribution in the states of FL, GA, LA, MI, NC and…Official notice →
  7. US
    Drugs & medicalClass II

    Mermaid Medical A/S recalls The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous catheter-based system available in 6 French. The disposable system…

    Internal product testing failed bubble leak testing (ASTM F2096), which indicates the sterility barrier may not be fully intact.

    FDA · DeviceMermaid Medical A/SWorldwide - US Nationwide distribution in the states of OH, MO, CO, NC, TX,…Official notice →
See all drugs & medical recalls →