ONE Snare® 00884450094945Recalls & reported problems
Merit Medical Systems, Inc. · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884450094945), received between Jul 18, 2023 and May 21, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Fracture2
- Material Integrity Problem1
- Material Separation1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 21, 2024Fracture; Material Separation; Fracture; Material Separation
THE ACCOUNT ALLEGES THAT DURING THE PROCEDURE, THE LOOP OF THE ONE SNARE DEVICE DETACHED DURING THE RETRIEVAL OF ANOTHER DEVICE. NO ADDITIONAL PATIENT CONSEQUENCE TO REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19360403 ↗InjuryJul 18, 2023Fracture; Material Integrity Problem; Fracture; Material Integrity Problem
THE ACCOUNT ALLEGES THAT DURING THE PROCEDURE, THE PT/IR MARKER OF THE CATHETER DETACHED AND MIGRATED TO THE POSTERIOR INFERIOR CEREBRAL ARTERY IN THE BRAIN. NO ADDITIONAL INFORMATION AVAILABLE.
Patient problems: Foreign Body In Patient
MAUDE report 17347417 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.