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Innervision 27065 CRecalls & reported problems

Medtronic Ps Medical, Inc. · CATHETER 27065 C VENT SNAP ENDO 6CM · Class 2 · Implant

Data updated Oct 13, 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 00643169483880), received between Jul 19, 2017 and Jul 19, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (1 report).

29 other recalls cover devices cleared under the same FDA submission (K983331); 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

  • Device Operates Differently Than Expected1

Patient problems

  • Therapeutic Response, Decreased1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 19, 2017Device Operates Differently Than Expected; Device Operates Differently Than Expected

    IT WAS REPORTED TO MEDTRONIC NEUROSURGERY THAT ON (B)(6) 2017, THE PHYSICIAN'S NOTES SHOWED THEY LEFT THE NEW VALVE AT THE PRIOR SETTING, BUT THE PATIENT WAS NOTED TO HAVE HYDROCEPHALUS. REPORTEDLY, THE PATIENT WENT TO SURGERY ON (B)(6) 2017 AND HAD A VENTRICULOPERITONEAL (VP) SHUNT REVISION. THE PHYSICIAN'S OPERATIVE NOTE STATED THEY DECIDED TO REPLACE THE VALVE AND CHANGE THE SETTING AS WELL AS REPLACE THE PROXIMAL CATHETER WITH ANOTHER CATHETER.

    Patient problems: Therapeutic Response, Decreased

    MAUDE report 6725983 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K983331. One submission often covers many models, so check the product and lot details in each record.

  • Z-1134-2009 · Feb 12, 2009 · Terminated
    Medtronic 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 · Terminated
    Snap 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-1125-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1124-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1142-2009 · Feb 12, 2009 · Terminated
    Snap 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-1133-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1127-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1135-2009 · Feb 12, 2009 · Terminated
    Snap 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 · Terminated
    Medtronic 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-1145-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1150-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1149-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1140-2009 · Feb 12, 2009 · Terminated
    Snap 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-1141-2009 · Feb 12, 2009 · Terminated
    Snap 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-1138-2009 · Feb 12, 2009 · Terminated
    Snap 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

…and 14 more.

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Sources and updates

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