Skip to content

Delta® 25014-5 (UDI 00643169472907)Recalls & reported problems

Medtronic Ps Medical, Inc. · SHUNT 25014-5 UNI DELTA SML · Class 2 · Implant

All models of Delta (31)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00643169472907), received between Feb 2, 2017 and Feb 2, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Occlusion Within Device” (1 report).

31 other recalls cover devices cleared under the same FDA submission (K792007); 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

  • Occlusion Within Device1

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.

  • MalfunctionFeb 2, 2017Occlusion Within Device; Occlusion Within Device

    IT WAS REPORTED TO MEDTRONIC NEUROSURGERY THAT THE PHYSICIAN PLACED THE DEVICE AND IT DID NOT DRAIN INTRA-OPERATIVELY. ACCORDING TO THE REPORT, AFTER 15 MINUTES, THE PHYSICIAN TRIED USING A SYRINGE AT THE DISTAL END, BUT THE DEVICE STILL DID NOT DRAIN. REPORTEDLY, THE DEVICE WAS REPLACED WITH ANOTHER MANUFACTURER¿S DEVICE AND THERE WAS NO INJURY TO THE PATIENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6298076 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K792007. One submission often covers many models, so check the product and lot details in each record.

  • Z-1117-2021 · Jan 11, 2021 · Open, Classified
    Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for the following CFNs: 22011 L- SHUNT 22011 L INTL ONLY ULTRA SM LOW 22011 LL - SHUNT 22011 LL INTL ONLY
  • Z-0397-2014 · Nov 18, 2013 · Terminated
    CSF-Unitized Shunt, Contoured Regular, Low Pressure, Catalog No. 46022; CSF-Unitized Shunt, Contoured Regular, Medium Pressure, Catalog No. 46024; CSF-Unitized Shunt, Contoured Reg
  • 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-1148-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1132-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1129-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1144-2009 · Feb 12, 2009 · Terminated
    Medtronic 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-1136-2009 · Feb 12, 2009 · Terminated
    Snap 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-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-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-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-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-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-1137-2009 · Feb 12, 2009 · Terminated
    Snap 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-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

…and 16 more.

Other Shunt, central nervous system and components devices

All Shunt, central nervous system and components devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page