Mirion recalls Captus 4000e Thyroid Uptake System with Well and 2 inch shielding due to reported unexpected detachment of the collimator, which could lead to radiation exposure risks during thyroid uptake procedures.
Complaints of unexpected detachment of the collimator have been reported.
Mirion is recalling its Captus 4000e Thyroid Uptake System with Well and 2 inch shielding because users have reported the collimator detaching unexpectedly. This could cause radiation exposure during thyroid uptake tests if not properly secured.
The collimator can detach unexpectedly during use, potentially leading to radiation exposure for the user or patient if the system is not securely attached. This risk is specific to thyroid uptake procedures where precise radiation measurement is critical.
Healthcare professionals using the Captus 4000e Thyroid Uptake System for thyroid uptake tests, staff bioassays, or wipe tests are affected. Those who use the system without proper anchoring are at higher risk.
Check for the Captus 4000e Thyroid Uptake System with Well and 2 inch shielding. The product has a serial number range from 940001 to 941398 and was sold with lot code 5430-30154.
Ensure the collimator is securely fastened before each use to prevent unexpected detachment.
Yes, if you have the Captus 4000e Thyroid Uptake System with Well and 2 inch shielding with a serial number between 940001 and 941398.
Stop using the system immediately and contact Mirion Technologies for guidance on safe handling and potential repairs.
The recall record does not specify a fix or remedy, so you should contact Mirion directly for assistance.
We’ve drafted a message you can send Mirion Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1894-2024 — Mirion Technologies Mirion Technologies Hello, I own a Mirion Technologies that is covered by recall Z-1894-2024 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.
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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.
