Drugs & medicalClass II

IBA Dosimetry GmbH recalls myQA iON; Article Number: MQ10-000;

Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.

Read the official notice →
Date
2025-05-07
Country
United States
Brand
IBA Dosimetry GmbH
Product
myQA iON; Article Number: MQ10-000;
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of AL, AR, FL, GA, KS,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-05-07
  2. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Numbers:…

    Preset treatment parameters are not consistently being used in accordance with the IFU.

    FDA · DeviceOlympus Corporation of the AmericasWorldwide distribution - US Nationwide and the countries of AU, CA, SG, DE,…Official notice →
  3. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits, labeled as: T AND A PACK -LF, REF DYNJ85792

    It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Panama and Canada.Official notice →
  4. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Enhanced Verify Evaluation Handset (CFN HH90130FA)

    Evaluation handsets may not be able to communicate with the neurostimulator due to handsets having a faster processing speed than prior handsets. An inability to connect may cause the therapy to stop being delivered…

    FDA · DeviceMedtronic NeuromodulationUS Nationwide distribution including in the states of AR, AZ, CA, CO, CT, FL,…Official notice →
  5. US
    Drugs & medicalClass II

    Waldemar Link GmbH & Co. KG (Mfg Site) recalls Posterior Femoral Augment; Item Numbers: (1) 880-310/11 (Sz. 0 - cemented sm), (2) 880-310/21 (Sz. 0 - cemented lg), (3)…

    The device was delivered with a preassembled Femoral Augment screw that was missing its thread.

    FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)US Nationwide distribution in the states of AL, AZ, CA, CO, FL, GA, IN, IL,…Official notice →
  6. US
    Drugs & medicalClass II

    Spectrum Medical Ltd. recalls Brand Name: Quantum Informatics - VIPER Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or Alarms) Product…

    Medical device software marketed without FDA clearance .

    FDA · DeviceSpectrum Medical Ltd.California, Florida, Illinois, Arkansas, Georgia, Wisconsin, Arizona,…Official notice →
  7. US
    Drugs & medicalClass II

    Defibtech, LLC recalls Semi-Automated External Defibrillators; Models: DDU-100 and DDU-100E. Item numbers: DCF-E110SG-DE/1 (German language), DCF-E110SG-FR/1…

    It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance (MedDO) states that product information (labelling and instructions for use) should be provided in…

    FDA · DeviceDefibtech, LLCInternational Only: Switzerland.Official notice →
See all drugs & medical recalls →