Halo™ Single Loop Snare Kit 383615120Recalls & reported problems
Argon Medical Devices, Inc. · Halo™ Single Loop Snare Kit 6F, 15mm x 120cm · 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 00886333224883), received between Mar 13, 2023 and Mar 13, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Separation” (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 Separation1
- Peeled/Delaminated1
- Separation Problem1
Patient problems
- Foreign Body In Patient1
- Insufficient Information1
- 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.
MalfunctionMar 13, 2023Peeled/Delaminated; Material Separation; Separation Problem; Peeled/Delaminated; Material Separation; Separation Problem
IT WAS REPORTED THAT DR. (B)(6) HAD SNARED A PORT AND CATHETER, THEN TRIED TO ADVANCE TO PORT WITH THE SNARE AND THE RADIOPAQUE MARKER BAND CAME OFF THE CATHETER. IT WAS RETRIEVED AND THE ENTIRE UNIT IS ABLE TO BE SENT BACK.
Patient problems: Foreign Body In Patient; Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16530875 ↗
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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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