MindFrame Capture LP Revascularization Devices: Product Numbers: — Class I medical device recall Z-1701-2018
Terminated recall by Micro Therapeutics Inc, Dba Ev3 Neurovascular, reported 2018-05-23. There is a potential issue for all MindFrame Capture devices to partially detach or separate from the delivery
| Recall number | Z-1701-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Micro Therapeutics Inc, Dba Ev3 Neurovascular, Irvine, CA, United States |
| Recall initiated | 2018-02-26 |
| Classified | 2018-05-16 |
| Reported by FDA | 2018-05-23 |
| Terminated | 2021-09-30 |
| Quantity | 1,942 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00843889031334, 00843889031341, 00843889031365, 00843889031372, 00843889031396, 00843889031402, 00843889031426, 00843889031433, 00847536020122, 00847536020139, 00847536020146, 00847536020153, 00847536020160, 00847536020177, 00847536020184, 00847536020191, 00847536020207, 00847536020214, 00847536020221, 00847536020238 |
| Model numbers | 00843889031334, 00843889031341, 00843889031365, 00843889031372, 00843889031396, 00843889031402, 00843889031426, 00843889031433, 00847536020122, 00847536020139, 00847536020146, 00847536020153, 00847536020160, 00847536020177, 00847536020184, 00847536020191, 00847536020207, 00847536020214, 00847536020221, 00847536020238, 300010, 300011, 300012, 300013, 300014 and 4 more |
Product
MindFrame Capture LP Revascularization Devices: Product Numbers: (a) REF 300010 (b) REF 300011 (c) REF 300012 (d) REF 300013 (e) REF 300014 (f) REF 300015 (g) REF 300016 (h) REF 300017 (i) REF 300018 Intended to restore blood flow by removing thrombus from a large intracranial vessel experiencing ischemic stroke within 8 hours of symptom onset.
Reason for recall
There is a potential issue for all MindFrame Capture devices to partially detach or separate from the delivery wire.
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-1701-2018. 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.