CaptureTM 300018 (UDI 00847536020191)Recalls & reported problems
Micro Therapeutics, Inc. · 300018 CAPTURE LP 3X20 US · Class 2
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's 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, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- 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 · FDA record ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.