---
title: "Captus 4000e Thyroid Uptake System. Intended to be used to perform Thyroid Up... — FDA record Z-1892-2024 | Is It on Recall"
description: "Complaints of unexpected detachment of the collimator have been reported."
url: https://isitonrecall.com/recall/fda-device-z-1892-2024-captus-4000e-thyroid-uptake-system-intended-to-be-used-to-perform-thyroid-uptakes-staff-bioassay-and/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Captus 4000e Thyroid Uptake System. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests. — FDA record Z-1892-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 22, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Captus 4000e Thyroid Uptake System. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.
- **Reason**: Complaints of unexpected detachment of the collimator have been reported.
- **Classification**: Class II
- **Recalling firm**: Mirion Technologies (Capintec), Inc.
- **Quantity**: 1,275 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1892-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1892-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot Code: Model No: 5430-30151; UDI 859942006096, S/N range 940001 through 941398. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US Nationwide distribution and the countries of ALGERIA, AUSTRALIA, AUSTRIA, BANGLADESH, CANADA, CHILE, CHINA, COSTA RICA, CROATIA, FRANCE, GERMANY, GUAM, HONDURAS, HUNGARY, INDIA, ISRAEL, ISREAL, ITALY, JAPAN, KOREA, LATVIA, MALAYSIA, NETHERLANDS, NEW ZEALAND, PAKISTAN, PHILIPPINES, PHILIPPINES , PHILLIPINES, PUERTO RICO, QATAR, SAUDI ARABIA, SERBIA, SOUTH AFRICA, SOUTH KOREA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, TAIWAN , THAILAND, TURKEY, UNITED KINGDOM, VIETNAM.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jun 5, 2024
- **Recall initiation date**: Apr 22, 2024
- **Center classification date**: May 24, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1892-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Mirion Technologies (Capintec), Inc. records](https://isitonrecall.com/brand/mirion-technologies-capintec-inc/)
