Mirion Technologies (Capintec), Inc.: Medical Device Recall in 2024 - (Recall #: Z-1069-2024)

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 Systems- Intended to be used by trained Nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures. Models: 5430-30151, 5430-30152, and 5430-30154

Product Classification:

Class II

Date Initiated: November 27, 2023

Date Posted: February 21, 2024

Recall Number: Z-1069-2024

Event ID: 93824

Reason for Recall:

Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the collimator to fall downward to its lowest point of travel, causing potential injury with a patient or operator

Status: Ongoing

Product Quantity: 467 units

Code Information:

UDI: 0859942006096 and 0859942006102 Serial Numbers: 940000 through 940535

Distribution Pattern:

Nationwide Foreign: AUSTRIA BANGLADESH BRASIL Brazil CANADA CHILE Costa Rica Ecuador France Hanoi Vietnam Hong Kong INDIA ISRAEL ITALY Malaysia PAKISTAN Philippines POLAND Saudi Arabia SOUTH KOREA Spain SWEDEN TAIWAN THAILAND TURKEY UNITED ARAB EMIATES UNITED KINGDOM VIETNAM

Voluntary or Mandated:

Voluntary: Firm initiated