Mirion Technologies (Capintec) recalls
Recall found. Mirion Technologies (Capintec) is named in FDA Class II recall Z-3193-2026 covering Captus 4000e Thyroid Uptake System.
Hazard: 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. Identifying details: Affected Units: Captus 4000: 1. Model 5430-30151; UDI-DI: 00859942006096; 2. Model 5430-30152; UDI-DI: 00859942006102; 3. Model 5430-30154; UDI-DI: 00859942006423; Devices shipped from April 2019 through February 2024, Serial Numbers 940548 through 941398, that have NOT already replaced the original arm with the redesigned arm.. Status: Ongoing.
Models with recalls
All Mirion Technologies (Capintec) recalls
FDA Class II · Medical device · September 23, 2026
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.
Official ID Z-3193-2026 ·
Official record ↗
Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.