N/A 41409Recalls & reported problems
Medtronic Ps Medical, Inc. · CATHETER 41409 CSF-VENT STD W/SNAP 9CM · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000029197), received between Nov 21, 2025 and Nov 21, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Disconnection” (1 report).
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
- Disconnection1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 21, 2025Disconnection; Disconnection
MEDTRONIC RECEIVED INFORMATION REGARDING A MAGNETIC RESISTANT ADJUSTABLE SHUNT. IT WAS REPORTED THAT THE SHUNT WAS PLACED ON (B)(6) 2025, AND IT WAS NOTICED ON (B)(6) 2025, THAT THE SNAP VENTRICULAR CATHETER HAD DETACHED FROM THE RICKHAM RESERVOIR. THE SURGEON TOOK THE PATIENT BACK TO SURGERY TO RETRIEVE THE CATHETER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23616480 ↗
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-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-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-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
- 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-1138-2009 · Feb 12, 2009 · TerminatedSnap Shunt Ventricular Catheter, Standard, with BioGlide, 7 CM, Ref 27708D. 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-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-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-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-1124-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782L. Sizes: 3 CM in length, REF (240) 27782L. Each catheter is provided in a sealed Tyvek plas
- 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-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-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-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-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
…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 41406Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular2 reports
- 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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