Mirion recalls Captus 4000e Thyroid Uptake Systems after reports of collimator detachment during use. Affected units have specific serial numbers and lot codes. Contact for return or repair instructions.
Complaints of unexpected detachment of the collimator have been reported.
Mirion is recalling its Captus 4000e Thyroid Uptake System due to reports of the collimator detaching unexpectedly. This could lead to safety issues during medical testing procedures.
The collimator, a part that directs radiation, can detach unexpectedly during use. This poses a risk of radiation exposure to staff or patients if the system is not properly secured.
Healthcare professionals using the Captus 4000e system for thyroid tests and staff bioassays are most at risk. The recall affects specific units with serial numbers from 940001 to 941398.
Check the serial number on the device, which ranges from 940001 to 941398. The product has a lot code and model number 5430-30152. It was sold with UDI 0859942006102.
Verify the serial number is between 940001 and 941398 to confirm if the device is affected.
Reach out to Mirion Technologies for instructions on returning or repairing the device.
The model number is 5430-30152.
Check the serial number, which ranges from 940001 to 941398. The product also has a lot code and UDI 0859942006102.
Contact Mirion Technologies for instructions on returning or repairing the device.
We’ve drafted a message you can send Mirion Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1893-2024 — Mirion Technologies Mirion Technologies Hello, I own a Mirion Technologies that is covered by recall Z-1893-2024 from Mirion Technologies. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
