IBA Dosimetry GmbH: Medical Device Recall in 2025 - (Recall #: Z-1703-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

myQA iON; Article Number: MQ10-000;

Product Classification:

Class II

Date Initiated: April 1, 2025

Date Posted: May 7, 2025

Recall Number: Z-1703-2025

Event ID: 96647

Reason for Recall:

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

Status: Ongoing

Product Quantity: 84 units (9US, 75 OUS)

Code Information:

Article Number: MQ10-000; UDI-DI: EIBAMQ010000;

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of AL, AR, FL, GA, KS, MD, OK and the countries of Algeria, Austria, Belgium, Czech Republic, Denmark, France, Germany, Ireland, Italy, Morocco, Norway, Poland, Slovakia, Spain, Israel, Kazakhstan, Kosovo, Libya, South Africa, Turkey, United Kingdom, Switzerland, Argentina, Brazil, Mexico, APAC: Indonesia, Japan, Peoples Republic of China, Philippines, South Korea, Thailand.

Voluntary or Mandated:

Voluntary: Firm initiated