N/A 41406Recalls & reported problems
Medtronic Ps Medical, Inc. · CATHETER 41406 CSF-VENT STD W/SNAP 6CM · Class 2 · Implant
Data updated Oct 16, 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 00763000028510), received between Apr 8, 2026 and Apr 22, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Disconnection” (2 reports).
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Disconnection2
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Unspecified Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 22, 2026Disconnection
MEDTRONIC RECEIVED INFORMATION REGARDING A CATHETER. IT WAS REPORTED THAT PER THE DOCTOR, THE DEVICE DISCONNECTED AND HAND TO BE EXPLANTED FROM THE PATIENT. AN EXTERNAL VENTRICULAR DRAIN (EVD) WAS PLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24952628 ↗InjuryApr 8, 2026Disconnection
MEDTRONIC RECEIVED INFORMATION REGARDING A SHUNT. IT WAS REPORTED THE SHUNT BECAME DISCONNECTED FROM THE RESERVOIR TO THE PERITONEAL CATHETER. THE DOCTOR WENT IN ON (B)(6) 2026 AND RECONNECTED IT. ON (B)(6) 2026, THE DOCTORS FOUND THAT THE SAME SHUNT WAS AGAIN DISCONNECTED AND INFECTED.
Patient problems: Unspecified Infection
MAUDE report 24820991 ↗
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-1128-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782G. Sizes 10cm in length, REF (240) 27782G. Each catheter is provided in a sealed Tyvek plast
- 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-1127-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782H. Sizes: 11 CM in length, REF (240) 27782H. Each catheter is provided in a sealed Tyvek pla
- Z-1129-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782F. Sizes: 9 CM in length, REF (240) 27782F. Each catheter is provided in a sealed Tyvek plas
- Z-1136-2009 · Feb 12, 2009 · TerminatedSnap Shunt Ventricular Catheter, Standard, with BioGlide, 5 CM, Ref 27708B. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar pouch. The
- 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-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
- 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-1149-2009 · Feb 12, 2009 · TerminatedMedtronic Snap Shunt Ventricular Catheter, Standard, with BioGlide, 8 CM, Ref 27802F. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar po
- Z-1130-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782E. Sizes: 8 CM in length, REF (240) 27782E. 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-1146-2009 · Feb 12, 2009 · TerminatedMedtronic Snap Shunt Ventricular Catheter, Standard, with BioGlide, 5 CM, Ref 27802C. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar po
- 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-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-1148-2009 · Feb 12, 2009 · TerminatedMedtronic Snap Shunt Ventricular Catheter, Standard, with BioGlide, 7 CM, Ref 27802E. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar po
…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
- NA 41406Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR2 reports
- NA 41407Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR2 reports
- N/A 41409Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular1 report
- Innervision 27065 CMedtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR1 report
- Innervision 27065 BMedtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR1 report
- NA 44102Medtronic 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 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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