FDA Device recall Z-1893-2024
Captus 4000e Thyroid Uptake System with Well
- FDA Device
- Class II
- ongoing
- Published 2024-06-05
On 2024-06-05 the FDA classified a Class II recall of Captus 4000e Thyroid Uptake System with Well by Mirion Technologies Capintec, citing complaints of unexpected detachment of the collimator have been reported.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1893-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-22 |
| Published | 2024-06-05 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Mirion Technologies Capintec |
| Distribution | US |
Product
Captus 4000e Thyroid Uptake System with Well. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.
Reason
Complaints of unexpected detachment of the collimator have been reported.
Identifiers
| code_info | Lot Code: Model No: 5430-30152; UDI 0859942006102; S/N range 940001 through 941398. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1893-2024%22
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