Drugs & medicalClass II

Virtual Radiologic Corp. recalls vRad PACS with Mammography

The error resulted in intermittent failure of current (primary) radiology study images not displaying to the interpreting teleradiologist.

Read the official notice →
Date
2023-08-02
Country
United States
Brand
Virtual Radiologic Corp.
Product
vRad PACS with Mammography
Classification
Class II
Units
US Nationwide distribution in the states of MD, MN, TN, FL, GA, TX, 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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

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

    MICROVENTION INC. recalls FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA, FRED3524, FRED3524-CA,…

    Intracranial aneurysm flow diverter device may be manufactured with an incorrect inner stent length and may not perform as intended.

    FDA · DeviceMICROVENTION INC.Worldwide - US Nationwide distribution including in the states of AZ, NY, FL,…Official notice →
  3. US
    Drugs & medicalClass II

    Beckman Coulter, Inc. recalls Ringed DxI Reaction Vessels (RVs)

    Beckman Coulter, Inc. is recalling Ringed DxI Reaction Vessels (RVs) as part of Unicel DxI Immunoassay System (600, 800 series). The reason for the recall is that the firm has identified 3 lots of RVs that failed an…

    FDA · DeviceBeckman Coulter, Inc.Worldwide - US Nationwide distribution in the states of CA, MA, TX, NJ, MI,…Official notice →
  4. US
    Drugs & medicalClass II

    Trexo Robotics Holdings Inc. recalls Trexo Device

    Electrical issues that could potentially render the device non-functional, give off electromagnetic influence to surrounding equipment, and risk of burns when in use.

    FDA · DeviceTrexo Robotics Holdings Inc.Worldwide distribution - US Nationwide and the countries of the Argentina,…Official notice →
  5. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be used as a device that transmits Ho:YAG laser energy from cleared…

    Manufactured with the incorrect component may result in lower power output and degradation or dimming of the aiming beam, leading to reduced efficiency of fiber performance. Continued use may cause overheating of the…

    FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  6. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs

    The case and each (i.e. packet) labels for the DYND3000xxP series do not include an expiration date, however, the lubricating jelly (MDS032280) included in the DYNDP3000xxP series is labeled with an expiration date.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the country of Bermuda.Official notice →
  7. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..

    When an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Manager software application was not…

    FDA · DeviceMedtronic NeuromodulationInternational distribution to the countries of Israel and Serbia.Official notice →
See all drugs & medical recalls →