# FDA recall Z-1069-2024

> **Mirion Technologies (Capintec), Inc.** · Class II · device recall initiated 2023-11-27.

## 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

## Reason for recall

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

## Distribution

Nationwide Foreign:  AUSTRIA BANGLADESH BRASIL Brazil CANADA CHILE Costa Rica Ecuador France Hanoi Vietnam Hong Kong INDIA ISRAEL ITALY Malaysia PAKISTAN Philippines POLAND Saudi Arabia SOUTH KOREA Spain SWEDEN TAIWAN THAILAND TURKEY UNITED ARAB EMIATES UNITED KINGDOM VIETNAM

## Key facts

- **Recall number:** Z-1069-2024
- **Recalling firm:** Mirion Technologies (Capintec), Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-27
- **Report date:** 2024-02-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Florham Park, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1069-2024

## Citation

> AI Analytics. FDA recall Z-1069-2024. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1069-2024. Source: US FDA. Licensed CC0.

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