Captus 4000e Thyroid Uptake Systems- Intended to be used by trained… — Class II medical device recall Z-1069-2024
Ongoing recall by Mirion Technologies (Capintec), Inc., reported 2024-02-21, distributed nationwide. Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the collimator to fall downward to its
| Recall number | Z-1069-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mirion Technologies (Capintec), Inc., Florham Park, NJ, United States |
| Recall initiated | 2023-11-27 |
| Classified | 2024-02-09 |
| Reported by FDA | 2024-02-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BD, BR, CA, CL, CR, EC, ES, FR, GB, HK, IL, IN, IT, KR, MY, PH, PK, PL, SA, SE, TH, TR, TW, VN |
| Quantity | 467 units |
| UPC / GTIN / UDI-DI | 00859942006096, 00859942006102 |
| Serial numbers | 940000 |
| Model numbers | 5430-30151, 5430-30152, 5430-30154 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1069-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.