MMXClass II

Device, Percutaneous Retrieval

Cardiovascular · 21 CFR 870.5150

MDR events398All time

Recalls1All time

Registered firms81Currently listed

510(k) clearances32All time

Recent MDR events

398 adverse event reports on file

INDY OTW VASCULAR RETRIEVERJul 28, 2026
MalfunctionCook Inc.1820334-2026-00766
Triple-Loop Snare Retrieval KitJul 27, 2026
InjuryArgon Medical Devices, Inc0001625425-2026-00993
GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SETJul 9, 2026
MalfunctionCook Inc1820334-2026-00726
AVEIR¿ RETRIEVAL SYSTEM CATHETERJul 8, 2026
MalfunctionAbbott Medical (crm-sylmar)2017865-2026-14378
GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SETJul 8, 2026
InjuryCook Inc1820334-2026-00724
BARD SNARE USJun 19, 2026
MalfunctionHeraeus Medical Components Llc3008988055-2026-00005
AVEIR¿ RETRIEVAL SYSTEM CATHETERJun 12, 2026
MalfunctionAbbott Medical (crm-sylmar)2017865-2026-12235
AVEIR¿ RETRIEVAL SYSTEM CATHETERJun 5, 2026
DeathAbbott Medical (crm-sylmar)2017865-2026-11770
CLOVERSNARE 4-LOOP VASCULAR RETRIEVERMay 29, 2026
MalfunctionCook Inc1820334-2026-00574
EN SNARE®May 28, 2026
InjuryMerit Medical Ireland9616662-2026-00019

Event type breakdown

Malfunction252

Injury136

Death7

Other2

Unspecified1

Most-reported manufacturers

Cook Inc126 Merit Medical Systems, Inc.30 Argon Medical Devices19 Vascular Solutions, Inc.17 St. Jude Medical, Inc.(crm-sylmar)14 Merit Medical Systems13 Heraeus Medical Components Llc12 Radius Medical Technologies, Inc.11

Recalls

1 recall events for this product code

Cook Inc.
TerminatedAug 27, 2014
CloverSnare 4-Loop Vascular Retrieval Snare.
This remedial action is the result of six product complaints associated with separation of the snare from the distal tip of the wire.
Z-2243-2014 · View FDA record ↗

Registered firms

81 firms currently registered for this product code

510(k) clearances

32 clearances for this product code