Snare, Surgical
General, Plastic Surgery · 21 CFR 878.4800
Recent MDR events
150 adverse event reports on file
- SNARE CAPTIVATOR COLD SNARE 10MM LP 240CMIFeb 26, 2026MalfunctionUnknownMW5184503
- SNAREJan 26, 2026InjuryUnkMW5182868
- COLD SNAREDec 29, 2025MalfunctionMicro-tech(nanjing) Co.,ltd.3004837686-2025-00013
- MICRO TECH COLD SNAREDec 2, 2025InjuryMicro-tech (nanjing) Co., Ltd.MW5179696
- SUTURE RETRIEVER (6)Jun 19, 2025MalfunctionSmith & Nephew, Inc.1219602-2025-01537
- LESIONHUNTER(TM) ROTATABLE NITINOL COLD SNAREMay 9, 2025MalfunctionMicro-tech(nanjing) Co.,ltd.3004837686-2025-00005
- LESION HUNTER ROTATABLE NITINOL COLD SNARE 10 MMApr 22, 2025MalfunctionMicro-tech (nanjing) Co., Ltd.MW5169419
- SNAREMar 24, 2025InjuryUnkMW5168092
- LESIONHUNTER(TM) ROTATABLE NITINOL COLD SNAREJan 16, 2025MalfunctionMicro-tech(nanjing) Co.,ltd.3004837686-2025-00001
- LESIONHUNTER(TM) ROTATABLE NITINOL COLD SNAREJan 16, 2025MalfunctionMicro-tech(nanjing) Co.,ltd.3004837686-2025-00002
Event type breakdown
Recalls
3 recall events for this product code
- Surgical Instrument Service And Savings, Inc.TerminatedJul 1, 2013
- ConMed Linvatec Spectrum II Suture Hook Crescent, Medium (Teal) 4.0 x 20.0mm. REF C6386 Lot 122592.
The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
Z-1624-2013 · View FDA record ↗ - Bard Peripheral Vascular IncTerminatedSep 4, 2008
Bard Recovery Cone Removal System, Catalog Numbers: RC-15. The device is intended for use for percutaneously remove the recovery filter or facilitate the retr
This action is being taken because the product has a potential for the handle to detach. The handle detachment may result in the device unable to retrieve the filter or foreign body.
Z-1854-2008 · View FDA record ↗ - Bard Peripheral Vascular IncTerminatedSep 4, 2008
Bard Recovery Cone Removal System, Catalog Numbers: FBRC. The device is intended for use for percutaneously remove the recovery filter or facilitate the retri
This action is being taken because the product has a potential for the handle to detach. The handle detachment may result in the device unable to retrieve the filter or foreign body.
Z-1855-2008 · View FDA record ↗
Registered firms
69 firms currently registered for this product code
Richard Wolf Gmbh
KNITTLINGEN Baden-Wurttemberg, DE
Midwest Sterilization Corp.
JACKSON, MO, US
Anodyne Surgical
O Fallon, MO, US
Deroyal Industries, Inc.
POWELL, TN, US
Scanlan International, Inc.
Saint Paul, MN, US
Surgical Technologies, Inc.
ST. PAUL, MN, US
Faga Medical Industria De Equipamentos E Instrumentos Medico Hospitalares Ltda Me
Bauru Sao Paulo, BR
Boen Healthcare Co., Ltd.
Suzhou Jiangsu, CN
Dimeda Instrumente Gmbh
TUTTLINGEN Baden-Wurttemberg, DE
Sterigenics Us Llc
Los Angeles, CA, US
Quest Medical, Inc.
ALLEN, TX, US
Isomedix Operations, Inc.
Libertyville, IL, US
Bothwin (beijing) Medical Technology Co., Ltd.
Beijng Beijing, CN
Andratec Gmbh
Koblenz Rhineland-Palatinate, DE
Peters Surgical International Co., Ltd
Bangkok Krung Thep Maha Nakhon, TH
Win Wings Corp.
SIALKOT Punjab, PK
Elmed, Inc.
Glendale Heights, IL, US
Industrias Apson S.a De C.v
AGUA PRIETA Sonora, MX
Acheron Instruments (pvt.) Ltd.
LAHORE Punjab, PK
Fortune Medical Instrument Corp.
Taoyuan City, TW
Dewimed Medizintechnik Gmbh
TUTTLINGEN Baden-Wurttemberg, DE
Falcon Surgical Co. (pvt.) Ltd.
Sialkot Punjab, PK
Coroneo, Inc.
MONTREAL, QC Quebec, CA
Sterigenics Us Llc
West Memphis, AR, US
Peters Surgical
BOULOGNE-BILLANCOURT Hauts-de-Seine, FR
510(k) clearances
4 clearances for this product code