Mirion Technologies recalls
3 official recalls and safety alerts involving Mirion Technologies since 2024-02, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Mirion Technologies or the relevant agency.
- 2026-09-23
US
Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;
Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from the ground.
FDA · DeviceMirion Technologies (Capintec), Inc.Worldwide distribution - US Nationwide and the countries of ALGERIA, AUSTRIA,…Official notice →- 2024-06-05
US
Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.
Complaints of unexpected detachment of the collimator have been reported.
FDA · DeviceMirion Technologies (Capintec), Inc.Worldwide - US Nationwide distribution and the countries of ALGERIA,…Official notice →- 2024-02-21
US
Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake Systems- Intended to be used by trained Nuclear Medicine Technologists or Nuclear Medicine…
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
FDA · DeviceMirion Technologies (Capintec), Inc.Nationwide Foreign: AUSTRIA BANGLADESH BRASIL Brazil CANADA CHILE Costa Rica…Official notice →