Captus 4000e Thyroid Uptake System with 2 in well 5430-30154Recalls & reported problems
Mirion Technologies (capintec), Inc. · The Captus 4000e is a PC based Thyroid Uptake System, on a ergonomically designed mobile stand. It includes a 1024 channel MCA, automated Quality Assurance, Thyroid Uptake Module, and Bioassay module. This model includes a well counter with 2 inch of lead shielding. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Jul 20, 2026Class IIOpen, Classified
Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from the ground.
Z-3193-2026 · Root cause: Device Design · Recall details · FDA record ↗
- Apr 22, 2024Class IIOpen, Classified
Complaints of unexpected detachment of the collimator have been reported.
Z-1894-2024 · Root cause: Device Design · Recall details · FDA record ↗
Other Probe, Uptake, Nuclear devices
- Captus 4000e Thyroid Uptake SystemMirion Technologies (capintec), Inc. · Probe, Uptake, Nuclear3 recalls5 reports
- Captus 4000e Thyroid Uptake System with Well Captus 4000e Thyroid System with WellMirion Technologies (capintec), Inc. · Probe, Uptake, Nuclear3 recalls4 reports
- neoprobe NPCU3Devicor Medical Products, Inc. · Probe, Uptake, Nuclear1 recall0 reports
- TruNode Surgical Gamma Probe 120-807605Hologic, Inc. · Probe, uptake, nuclear11 reports
- GAMMA FINDER® IIIW.O.M. World of Medicine GmbH · Probe, Uptake, Nuclear1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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