Mirion Technologies (Capintec) recalls

Mirion Technologies (Capintec) has 4 recalls on record with the FDA and USDA, the earliest in 2024 and the latest reported on 5 Jun 2024. 4 are still ongoing. The most frequent reason is potency & assay.

Total recalls4since 2024

Last 12 months0reported

Class I00% of total

Ongoing4latest 5 Jun 2024

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 4 100%Class III 0 0%

Why mirion technologies (capintec) is recalled

Potency & Assay375%
Device Malfunction125%

Product types

Test Kits & Diagnostics375%
Other Medical Devices125%

By year

20244100%

Ongoing mirion technologies (capintec) recalls

4 active

Reported	Class	Recall	Company	Reason	Where
5 Jun 2024Device	CLASS II	Captus 4000e Thyroid Uptake System with Well and shielding recalled	Mirion Technologies (Capintec)	Potency & Assay	Nationwide
5 Jun 2024Device	CLASS II	Captus 4000e Thyroid Uptake System with Well recalled	Mirion Technologies (Capintec)	Potency & Assay	Nationwide
5 Jun 2024Device	CLASS II	Captus 4000e Thyroid Uptake System recalled	Mirion Technologies (Capintec)	Potency & Assay	Nationwide
21 Feb 2024Device	CLASS II	Captus 4000e Thyroid Uptake Systems- Intended to be used recalled	Mirion Technologies (Capintec)	Device Malfunction	Nationwide

All mirion technologies (capintec) recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
5 Jun 2024Device	CLASS II	Captus 4000e Thyroid Uptake System with Well and shielding recalled	Mirion Technologies (Capintec)	Potency & Assay	Nationwide
5 Jun 2024Device	CLASS II	Captus 4000e Thyroid Uptake System with Well recalled	Mirion Technologies (Capintec)	Potency & Assay	Nationwide
5 Jun 2024Device	CLASS II	Captus 4000e Thyroid Uptake System recalled	Mirion Technologies (Capintec)	Potency & Assay	Nationwide
21 Feb 2024Device	CLASS II	Captus 4000e Thyroid Uptake Systems- Intended to be used recalled	Mirion Technologies (Capintec)	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.