Innervision 27065 BRecalls & reported problems
Medtronic Ps Medical, Inc. · CATHETER 27065 B VENT SNAP ENDO 5CM · 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 00643169483897), received between Apr 13, 2020 and Apr 13, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Fracture1
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.
InjuryApr 13, 2020Fracture; Fracture
ADDITIONAL INFORMATION RECEIVED REPORTED THAT THERE WERE NO ENVIRONMENTAL/EXTERNAL/PATIENT FACTORS THAT MAY HAVE LED OR CONTRIBUTED TO THE ISSUE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9954955 ↗
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-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-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-1151-2009 · Feb 12, 2009 · TerminatedMedtronic Snap Shunt Ventricular Catheter, Standard, with BioGlide, 10 CM, Ref 27802H. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar p
- Z-1131-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782D. Sizes: 7 CM in length, REF (240) 27782D. Each catheter is provided in a sealed Tyvek plas
- 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-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-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-1132-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782C. Sizes: 6 CM in length, REF (240) 27782C. Each catheter is provided in a sealed Tyvek plas
- 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-1126-2009 · Feb 12, 2009 · TerminatedMedtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782J. Sizes: 4.5 CM in length, REF (240) 27782J. Each catheter is provided in a sealed Tyvek pl
- 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-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-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-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-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
…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
- N/A 41409Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular1 report
- Innervision 27065 CMedtronic 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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