Atrieve™ Vascular Snare Kit 382006015Recalls & reported problems
Argon Medical Devices, Inc. · Atrieve™ Vascular Snare Kit 6F · Class 2
Data updated Oct 16, 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 20886333004021), received between Jul 11, 2022 and Jul 11, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Fell” (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 16, 2026.
Most reported problems
Device problems
- Device Fell1
- Entrapment of Device1
Patient problems
- Device Embedded In Tissue or Plaque1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 11, 2022Entrapment of Device; Device Fell
DURING THE PRE-TEST THE FUNCTION OF THE ATRIEVE¿ VASCULAR SNARE IS OK, BUT WHEN THE OPERATORS WERE PUTTING THE ATRIEVE¿ VASCULAR SNARE IN THE VESSEL THEY FOUND THE COIL WAS KEEPING FALLING FROM THE LOOP, SO THE OPERATOR JUST IMMEDIATELY TOOK THE ATRIEVE¿ VASCULAR SNARE OUT. BECAUSE THIS PATIENT'S CONDITION IS UNSTABLE AND VERY BAD, SO THEY COULDN'T CONTINUOUS USE ANOTHER NEW VASCULAR SNARE TO TAKE THOSE FALLING COILS OUT. THE PHYSICIAN IS VERY UPSET ABOUT THE FALLING COILS. PLEASE NOTED THE FALLING COILS ARE STILL LEFT IN THIS PATIENT'S VESSEL NOW.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 14976766 ↗
Other Device, Percutaneous Retrieval devices
- Gunther Tulip G13287Cook Incorporated · Device, percutaneous retrieval1 death98 reports
- CloverSnare G53008Cook Incorporated · Device, percutaneous retrieval32 reports
- Indy OTW G51836Cook Incorporated · Device, percutaneous retrieval17 reports
- Aveir™ LSCR111St. Jude Medical, Inc. · Device, percutaneous retrieval2 deaths15 reports
- Bard Snare OUS SRK35Heraeus Medical Components LLC · Device, Percutaneous Retrieval13 reports
- Indy OTW G51835Cook Incorporated · Device, percutaneous retrieval8 reports
- EN Snare® 00884450452462Merit Medical Systems, Inc. · Device, percutaneous retrieval7 reports
- EN Snare® 00884450452479Merit Medical Systems, Inc. · Device, percutaneous retrieval6 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 16, 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