Recall Z-3193-2026— Mirion Technologies (Capintec), Inc.

Name: FDA recall Z-3193-2026
Creator: U.S. Food and Drug Administration
Published: 2026-07-20

Class II · Ongoing

Class II FDA medical device recall by Mirion Technologies (Capintec), Inc., initiated 2026-07-20. FDA's recall record names no specific 510(k) clearance for this event. Product: Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;. Reason: 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..

Recalling firm: Mirion Technologies (Capintec), Inc.
Classification: Class II
Status: Ongoing
Initiated: 2026-07-20
Firm location: Florham Park, NJ, United States

Product description

Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;

Reason for recall

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.