ClosureFast IS-7F11Recalls & reported problems
Covidien LP · Introducer Sheath Set · Class 2
All models of ClosureFast (6)
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 10884521140301), received between Jul 2, 2020 and Jul 2, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
5 other recalls cover devices cleared under the same FDA submission (K780126); they may or may not involve this specific model.
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
- Break1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 2, 2020Break
PHYSICIAN INTENDED TO USE A 7FR INTRODUCER SHEATH SET DURING TREATMENT OF THE PATIENT¿S GREAT SAPHENOUS VEIN (GSV). IFU WAS FOLLOWED. IT IS REPORTED THE GUIDEWIRE INSIDE THE INTRODUCER SHEATH BROKE WHILE STILL IN THE VEIN AND HAD TO BE SURGICALLY REMOVED. ALL PIECES WERE ACCOUNTED FOR. A NEW 7FR INTRODUCER SHEATH SET WAS THEN USED TO COMPLETE THE PROCEDURE. NO FURTHER PATIENT INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10227422 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K780126. One submission often covers many models, so check the product and lot details in each record.
- Z-2705-2026 · Jun 1, 2026 · Open, ClassifiedOne-Piece Introducer Tray, REF: 497455, 497434 cardiovascular
- Z-2806-2020 · Jun 19, 2020 · TerminatedClosureFast Micro Introducer Sheath Set, REF MIS-7F11; 7Fr/Ch (2.3mm)x11 cm. STERILE|EO; Rx ONLY - Product Usage: Introducer Products are stand-alone components, standard kits, or
- Z-1938-2020 · Apr 8, 2020 · TerminatedPAC Tray/5 Catheter Introducer Tray 8F, Model 497424, Rx Only, STERILE EO, UDI: 00886333214440 - Product Usage: The introducers are indicated for use in arterial and venous procedu
- Z-1029-2016 · Feb 17, 2016 · TerminatedClosureFast Micro Introducer Sheath Set 7Fr/Ch(2.3mm) x 7 cm REF MIS-F707 and ClosureFast Introducer Sheath Set 7Fr/Ch(2.3mm) x 11 cm REF IS-7F11. Indicated for use in arterial and
- Z-0764-2010 · Jan 6, 2009 · TerminatedPercutaneous Catheter Introducer Set, VNUS Medical Technologies Cath Shth Intro 7F x 7cm, catalog number IS-7F07, Disposable, Single Use, Do Not Re-sterilize, Manufactured in USA f
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- TandemLife 5740-2417Cardiacassist, Inc. · Dilator, Vessel, For Percutaneous Catheterization2 recalls0 reports
- TightRail Rotating Dilator Sheath 545-513Spectranetics Corporation · Dilator, Vessel, For Percutaneous Catheterization20 deaths74 reports
- VersaCross Connect LAAC Access Solution VXAK0003Baylis Médicale Cie Inc · Dilator, Vessel, For Percutaneous Catheterization2 deaths70 reports
- VersaCross Connect LAAC Access Solution VXAK0007Baylis Médicale Cie Inc · Dilator, Vessel, For Percutaneous Catheterization2 deaths54 reports
- AVANTI 504656XCordis Corporation · DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION1 recall2 reports
- Abiomed® 00884450732311Merit Medical Systems, Inc. · Dilator, Vessel, For Percutaneous Catheterization1 recall1 report
- Mini Stick MAX H965457510Angiodynamics, Inc. · DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION1 recall1 report
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.
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