Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Captus 4000e Thyroid Uptake Systems- Intended to be used by Recalled by Mirion Technologies (Capintec), Inc. Due to Spring arm failure with Captus 4000e Thyroid Uptake...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mirion Technologies (Capintec), Inc. directly.
Affected Products
Captus 4000e Thyroid Uptake Systems- Intended to be used by trained Nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures. Models: 5430-30151, 5430-30152, and 5430-30154
Quantity: 467 units
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mirion Technologies (Capintec), Inc.
Mirion Technologies (Capintec), Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report