Mirion Technologies (Capintec), Inc.: Medical Device Recall in 2024 - (Recall #: Z-1893-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Captus 4000e Thyroid Uptake System with Well. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.

Product Classification:

Class II

Date Initiated: April 22, 2024

Date Posted: June 5, 2024

Recall Number: Z-1893-2024

Event ID: 94570

Reason for Recall:

Complaints of unexpected detachment of the collimator have been reported.

Status: Ongoing

Product Quantity: 1,275 units

Code Information:

Lot Code: Model No: 5430-30152; UDI 0859942006102; S/N range 940001 through 941398.

Distribution Pattern:

Worldwide - US Nationwide distribution and the countries of ALGERIA, AUSTRALIA, AUSTRIA, BANGLADESH, CANADA, CHILE, CHINA, COSTA RICA, CROATIA, FRANCE, GERMANY, GUAM, HONDURAS, HUNGARY, INDIA, ISRAEL, ISREAL, ITALY, JAPAN, KOREA, LATVIA, MALAYSIA, NETHERLANDS, NEW ZEALAND, PAKISTAN, PHILIPPINES, PHILIPPINES , PHILLIPINES, PUERTO RICO, QATAR, SAUDI ARABIA, SERBIA, SOUTH AFRICA, SOUTH KOREA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, TAIWAN , THAILAND, TURKEY, UNITED KINGDOM, VIETNAM.

Voluntary or Mandated:

Voluntary: Firm initiated