AxiumTM FC-5-20-3DRecalls & reported problems
Micro Therapeutics, Inc. · FRAMING COIL FC-5-20-3D V01 · Class 2 · Implant
All models of AxiumTM (139)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00847536022966), received between Dec 5, 2019 and Dec 5, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
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.
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Foreign Body In Patient1
- Therapeutic Response, Decreased1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 5, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
MEDTRONIC RECEIVED REPORT THAT THE FRAMING COIL UNINTENTIONALLY DETACHED. THIS EVENT WAS TREATED BY PLACING A STENT AND ADHERING THE COIL TO THE VESSEL WALL. THE PATIENT WAS ALSO PLACED ON ASPIRIN. THERE WAS NO FRICTION DURING THE DELIVERY. THE COIL WAS NOT REPOSITIONED. A CONTINUOUS FLUSH WAS USED. IT IS UNKNOWN IF THE DEVICES WAS PREPARED AND USED PER THE INSTRUCTIONS FOR USE (IFU). ANCILLARY DEVICE: 6F SOPHIA THIS EVENT OCCURRED DURING THE TREATMENT OF A RUPTURED ICA, BASILAR ANEURYSM THAT WAS 6.5MM X 3.5MM AND 2.5MM NECK. NO ADDITIONAL IN FORMATION IS KNOWN.
Patient problems: Foreign Body In Patient; Therapeutic Response, Decreased
MAUDE report 9419294 ↗
Other DEVICE, NEUROVASCULAR EMBOLIZATION devices
- POD RBYPODJ60-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION355 reports
- Penumbra System SCH1Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION295 reports
- RUBY Coil RBY4C0860-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION276 reports
- Smart Coil 400SMTHXSFT0208Penumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION165 reports
- Penumbra System RH1-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION154 reports
- Optima Coil System OPTI0208CSS10Balt USA LLC · Device, Neurovascular Embolization3 recalls3 reports
- POD RBYPOD6-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION148 reports
- POD RBYPODJ30-APenumbra, Inc. · DEVICE, NEUROVASCULAR EMBOLIZATION132 reports
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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page