CaptureTMRecalls & reported problems across all models
Micro Therapeutics, Inc. · 8 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 8 models of CaptureTM by Micro Therapeutics, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
CaptureTM recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Feb 26, 2018Terminated
There is a potential issue for all MindFrame Capture devices to partially detach or separate from the delivery wire.
Z-1701-2018 · Root cause: Process design · names 8 of these models · Recall details · FDA record ↗
CaptureTM models
8 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CaptureTM 300015CATHETER, THROMBUS RETRIEVER1 recall0 reports
- CaptureTM 300016CATHETER, THROMBUS RETRIEVER1 recall0 reports
- CaptureTM 300017CATHETER, THROMBUS RETRIEVER1 recall0 reports
- CaptureTM 300018CATHETER, THROMBUS RETRIEVER1 recall0 reports
- CaptureTM 300015CATHETER, THROMBUS RETRIEVER1 recall0 reports
- CaptureTM 300016CATHETER, THROMBUS RETRIEVER1 recall0 reports
- CaptureTM 300017CATHETER, THROMBUS RETRIEVER1 recall0 reports
- CaptureTM 300018CATHETER, THROMBUS RETRIEVER1 recall0 reports
Other Micro Therapeutics, Inc. products
- PipelineTM Flex Embolization Device with Shield TechnologyTM79 models · 1,020 reports
- AxiumTM139 models · 832 reports · 1 recall
- PIPELINE114 models · 622 reports · 1 recall
- Concerto Detachable Coil System34 models · 595 reports
- Axium Prime Detachable Coil System70 models · 497 reports
- ConcertoTM70 models · 436 reports
- EchelonTM5 models · 225 reports · 2 recalls
- Axium Detachable Coil System69 models · 288 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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