Medical DeviceJun 5, 2024
Mirion Technologies (Capintec) Captus 4000e Thyroid Uptake System recall — FDA Z-1892-2024
Complaints of unexpected detachment of the collimator have been reported.
Class IIFDA: OngoingMirion Technologies (Capintec), Inc.
Recall history in this database
Classification mix: Class II: 4.
Medical DeviceJun 5, 2024
Mirion Technologies (Capintec) Captus 4000e Thyroid Uptake System with Well recall — FDA Z-1893-2024
Complaints of unexpected detachment of the collimator have been reported.
Class IIFDA: OngoingMirion Technologies (Capintec), Inc.
Medical DeviceJun 5, 2024
Mirion Technologies (Capintec) Captus 4000e Thyroid Uptake System with Well and 2 inch recall — FDA Z-1894-2024
Complaints of unexpected detachment of the collimator have been reported.
Class IIFDA: OngoingMirion Technologies (Capintec), Inc.
Medical DeviceFeb 21, 2024
Mirion Technologies (Capintec) Captus 4000e Thyroid Uptake Systems- Intended to be used by recall — FDA Z-1069-2024
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
Class IIFDA: OngoingMirion Technologies (Capintec), Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Mirion Technologies (Capintec), Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.