Mirion recalls Captus 4000e Thyroid Uptake Systems due to reported collimator detachment. Affected units have specific lot codes and serial numbers. Stop using immediately to prevent potential injury.
Complaints of unexpected detachment of the collimator have been reported.
Mirion recalls the Captus 4000e Thyroid Uptake System after reports of the collimator detaching unexpectedly. This could lead to injury during use, so affected users should stop using the device immediately.
The collimator can detach unexpectedly during use, which may cause injury. This device is used in medical settings where safety is critical, so detachment could lead to harm.
Healthcare professionals using the Captus 4000e system for thyroid tests, staff bioassays, or wipe tests are most at risk. The recall affects specific units with lot codes and serial numbers.
Check for the model number 5430-30151 on the device. Affected units have a serial number range from 940001 to 941398 and lot code UDI 859942006096.
The Captus 4000e Thyroid Uptake System should be stopped using now to prevent potential injury from collimator detachment.
The model number is 5430-30151.
Serial numbers range from 940001 to 941398.
Check for the model number 5430-30151 and serial numbers between 940001 and 941398.
We’ve drafted a message you can send Mirion Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1892-2024 — Mirion Technologies Mirion Technologies Hello, I own a Mirion Technologies that is covered by recall Z-1892-2024 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.
