NA 41406Recalls & reported problems
Medtronic Ps Medical, Inc. · CATHETER 41406 CSF-VENT STD W/SNAP 6CM · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00643169472327), received between Dec 12, 2017 and Dec 12, 2017 — classified as 2 injuries.
29 other recalls cover devices cleared under the same FDA submission (K874498); 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Inflammation2
- Sepsis2
- Staphylococcus Aureus2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 12, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ADDITIONAL INFORMATION RECEIVED REPORTED THE CAUSE OF THE INFECTION WAS UNKNOWN. IT WAS ALSO STATED THE INFECTION WAS SEPSIS. THE CURRENT STATUS OF THE PATIENT WAS REPORTEDLY UNKNOWN.
Patient problems: Inflammation; Sepsis; Staphylococcus Aureus
MAUDE report 7108432 ↗InjuryDec 12, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ADDITIONAL INFORMATION RECEIVED REPORTED THE CAUSE OF THE INFECTION WAS UNKNOWN. IT WAS ALSO STATED THE INFECTION WAS SEPSIS. THE CURRENT STATUS OF THE PATIENT WAS REPORTEDLY UNKNOWN.
Patient problems: Inflammation; Sepsis; Staphylococcus Aureus
MAUDE report 7108388 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K874498. One submission often covers many models, so check the product and lot details in each record.
- Z-1143-2009 · Feb 12, 2009 · TerminatedSnap Shunt Ventricular Catheter, Standard, with BioGlide, 11 CM, Ref 27708J Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar pouch. The
- Z-1152-2009 · Feb 12, 2009 · TerminatedMedtronic Snap Shunt Ventricular Catheter, Standard, with BioGlide, 11 CM, Ref 27802J. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar p
- Z-1142-2009 · Feb 12, 2009 · TerminatedSnap Shunt Ventricular Catheter, Standard, with BioGlide, 10 CM, Ref 27708H. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar pouch. The
- Z-1134-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782A. Sizes: 4 CM in length, REF (240) 27782 a. Each catheter is provided in a sealed Tyvek pla
- Z-1133-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782B. Sizes: 5 CM in length, REF (240) 27782B. Each catheter is provided in a sealed Tyvek plas
- Z-1135-2009 · Feb 12, 2009 · TerminatedSnap Shunt Ventricular Catheter, Standard, with BioGlide, 4 CM, Ref 27708A. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar pouch. The
- Z-1150-2009 · Feb 12, 2009 · TerminatedMedtronic Snap Shunt Ventricular Catheter, Standard, with BioGlide, 9 CM, Ref 27802G. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar po
- Z-1144-2009 · Feb 12, 2009 · TerminatedMedtronic Snap Shunt Ventricular Catheter, Standard, with BioGlide, 3 CM, Ref 27802A. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar po
- Z-1145-2009 · Feb 12, 2009 · TerminatedMedtronic Snap Shunt Ventricular Catheter, Standard, with BioGlide, 4 CM, Ref 27802B. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar po
- Z-1125-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782K. Sizes:5.5CM in length, REF (240) 27782K. Each catheter is provided in a sealed Tyvek plas
- Z-1140-2009 · Feb 12, 2009 · TerminatedSnap Shunt Ventricular Catheter, Standard, with BioGlide, 3 CM, Ref 27708F. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar pouch. The
- Z-1137-2009 · Feb 12, 2009 · TerminatedSnap Shunt Ventricular Catheter, Standard, with BioGlide, 6 CM, Ref 27708C. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar pouch. The
- Z-1147-2009 · Feb 12, 2009 · TerminatedMedtronic Snap Shunt Ventricular Catheter, Standard, with BioGlide, 6 CM, Ref 27802D. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar po
- Z-1141-2009 · Feb 12, 2009 · TerminatedSnap Shunt Ventricular Catheter, Standard, with BioGlide, 9CM, Ref 27708G. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar pouch. The s
- Z-1139-2009 · Feb 12, 2009 · TerminatedSnap Shunt Ventricular Catheter, Standard, with BioGlide, 8 CM, Ref 27708E. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar pouch. The
…and 14 more.
Other PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR devices
- N/A 44010Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular30 reports
- NA 44010Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR9 reports
- N/A 41406Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular2 reports
- NA 41407Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR2 reports
- NA 27051Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR1 report
- NA 44102Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR1 report
- Innervision 27065 BMedtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR1 report
- N/A 41409Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular1 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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