Magic Infusion Catheter MA1.5FOLIVEMPRecalls & reported problems
Balt USA LLC · Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00818053022838), received between Sep 26, 2024 and Sep 26, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Rupture” (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.
Reports received per month
Most reported problems
Device problems
- Material Rupture1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 26, 2024Material Rupture; Material Rupture
IT WAS REPORTED THAT: "THE PHYSICIAN WAS USING MAGIC IN A RUPTURED AVM. MAGIC WAS PLACED IN APPROPRIATE VESSEL. ANGIO WAS PERFORMED. STARTED TO DELIVER GLUE NBCA. THEY SAW GLUE COME OUT OF THE MIDDLE OF THE CATHETER AND TRAVEL DISTAL. HAPPENED ALL OF A SUDDEN. THEY REMOVED THE CATHETER AND CONTINUED THE TREATMENT WITH ANOTHER CATHETER. IT IS HARD TO KNOW IF THERE WAS ANY PATIENT INJURY TO RUPTURED CATHETER. THE AVM WAS RUPTURED BEFORE HAND. PATIENT WAS REALLY SICK. HE WAS USING A 3CC SYRINGE FOR INJECTIONS." INCIDENT REPORT FORM SUBMITTED FOR THIS COMPLAINT INDICATES THAT NO PATIENT INJURY WAS SUSTAINED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20314139 ↗
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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.
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