Mirion Technologies (Capintec), Inc. 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 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Mirion Technologies (Capintec), Inc.
Lot Codes / Batch Numbers
UDI: 0859942006096 and 0859942006102 Serial Numbers: 940000 through 940535
Products Sold
UDI: 0859942006096 and 0859942006102 Serial Numbers: 940000 through 940535
Mirion Technologies (Capintec), Inc. is recalling Captus 4000e Thyroid Uptake Systems- Intended to be used by trained Nuclear Medicine Technologists o due to Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the collimator to fall downward to its lowest point of travel, causing potentia. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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
Recommended Action
Per FDA guidance
Capintec issued Product Urgent Safety Alert Preventative Action letter on 11/27/23 via email. Letter states reason for recall, health risk, and action to take: 1. Review this Alert and ensure that all affected personnel, including all operators of Captus 4000e Thyroid Uptake Systems, are aware of the contents. 2. Instruct affected personnel and operators to comply with the following steps in the interest of patient and operator safety: a. Prior to moving the arm, ensure that the positioning locks are released. b. Use caution when moving the spring arm vertically. Ensure that when the spring arm is moved vertically, the operator and patient are not below the spring arm or in its travel path. Move the spring arm using an outstretched arm, ensuring no body parts are in the spring arm s travel path. c. Once in position, secure the arm by tightening the locking handle prior to performing Thyroid Uptake and Bioassay Procedures. d. Perform Thyroid Uptake and Bioassay Procedures with patient (or employee, for Bioassay Procedures) in a seated position, rather than a supine position on a table. e. Store the arm in an upright position. This places the least amount of stress on the internal components. Engage the locking handle when the spring arm is not being raised or lowered. If you have any questions about this Safety Alert, the Preventive Action steps outlined above, or your Captus 4000e Thyroid Uptake System, please contact Capintec Customer Support at the phone number or email listed below. If you notice any unusual change in the performance or functional response of the arm in your system (e.g. arm is making an unusual noise or arm does not move smoothly at any articulation joint), please contact Capintec Customer Support: Capintec Customer Support: 1-800-631-3826 (201) 825-9500 CapintecSupport@mirion.com
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026