Mirion Technologies (Capintec), Inc. recalls
Every recall we track for Mirion Technologies (Capintec), Inc. — 5 in all, from 2023–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Mirion Technologies (Capintec), Inc. peaked in 2024 (3); 5 since 2017. 20% rated “stop using now”.
All FDA recall records for Mirion Technologies (Capintec), Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 1 | 0 | 0 | 1 |
| 2024 | 1 | 2 | 0 | 0 | 3 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
Most common reasons for Mirion Technologies (Capintec), Inc. recalls
What to do if you have a recalled Mirion Technologies (Capintec), Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Mirion Technologies (Capintec), Inc. recalls
3 shown- Use cautionMedical device
Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;
Mirion recalls Captus 4000e Thyroid Uptake Systems (models 5430-30151, 5430-30152, 5430-30154) due to potential tension bolt failure causing spring arm to drop 25 inches. Affected units shipped April 2019–Feb 2024 with serial numbers 940548–941398.
MirionJul 20, 2026 - Stop using nowMedical device
Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.
Mirion recalls Captus 4000e Thyroid Uptake Systems due to reported collimator detachment. Affected units have specific lot codes and serial numbers. Stop using immediately to prevent potential injury.
Mirion TechnologiesApr 22, 2024 - Use cautionMedical device
Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake Systems- Intended to be used by trained Nuclear Medicine Technologists or Nuclear Medicine
Mirion recalls Captus 4000e Thyroid Uptake Systems due to spring arm failure that may cause collimator to fall, potentially injuring patients or operators. Affected models include 5430-30151, 5430-30152, and 5430-30154 with serial numbers 940000-940535.
Mirion TechnologiesNov 27, 2023
Mirion Technologies (Capintec), Inc. recall questions
How many recalls has Mirion Technologies (Capintec), Inc. had?
5 recalls from Mirion Technologies (Capintec), Inc. are on record with U.S. safety agencies, from 2023–2026.
What is the most recent Mirion Technologies (Capintec), Inc. recall?
Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;, dated Jul 20, 2026. Every Mirion Technologies (Capintec), Inc. recall is listed on this page, newest first.
Why are Mirion Technologies (Capintec), Inc. products recalled?
The most common reasons on record: Complaints of unexpected detachment of the collimator have been reported. (3).
What should I do if I have a recalled Mirion Technologies (Capintec), Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Mirion Technologies (Capintec), Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.