VIA Microcatheter VIA-27-154-01Recalls & reported problems
Sequent Medical, Inc. · VIA 27 Microcatheter · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00851566003420), received between Nov 9, 2021 and Feb 23, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (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
- Material Split, Cut or Torn1
- Peeled/Delaminated1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 23, 2022Peeled/Delaminated; Peeled/Delaminated
IT WAS REPORTED THAT DURING A PROCEDURE FOR THE TREATMENT OF A CAROTID SIPHON ANEURYSM WITH UNFAVORABLE ANATOMY, A WEB DEVICE FAILED PLACEMENT AND GOT STUCK IN THE VIA 27 MICROCATHETER. THE PHYSICIAN DECIDED TO REMOVE ALL THE DEVICES ALL AT ONCE. REPORTEDLY, THE VIA 27 WAS DELAMINATED. THE PHYSICIAN USED A SECOND VIA MICROCATHETER AND A SECOND WEB AND THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT ANY PROBLEM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13587354 ↗MalfunctionNov 9, 2021Material Split, Cut or Torn; Material Split, Cut or Torn
IT WAS REPORTED THAT A WEB DEVICE WAS USED TO TREAT A WIDE-NECKED BASILAR TIP ANEURYSM. A VIA 27 PLACED INTO ANEURYSM. A WEB WAS DEPLOYED SUCCESSFULLY ON FIRST ATTEMPT INTO ANEURYSM; HOWEVER, A DECISION WAS TAKEN TO CHANGE THE SIZE. THE ORIGINAL WEB WAS RESHEATHED; HOWEVER, FRICTION WAS ENCOUNTERED. THE PARTIALLY DEPLOYED WEB/VIA SYSTEM WAS WITHDRAWN INTO A GUIDE CATHETER AND REMOVED FROM THE PATIENT. A NEW VIA 27 MICROCATHETER WAS TAKEN AND PLACED IN THE ANEURYSM, A WEB WAS SUCCESSFULLY DEPLOYED AND IMPLANTED. ON FIRST INSPECTION THE VIA 27 HAD A SPLIT OUTER COATING AND INTACT INNER CATHETER. THERE WAS NO REPORT OF ANY COATING PARTS LEFT IN THE PATIENT, AND NO REPORT OF HARM OR INJURY TO THE PATIENT, WHO IS DOING WELL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12782807 ↗
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- Chameleon CH08-40-75USMozarc Medical US LLC · Catheter, continuous flush2 recalls4 reports
- RebarTM 105-5081-153Micro Therapeutics, Inc. · Catheter, continuous flush2 deaths102 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.
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