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Delta® 24027-1Recalls & reported problems

Medtronic Ps Medical, Inc. · ASSY 24027-1 DELTA SHUNT SNAP SML 1 · 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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00643169497177), received between May 31, 2017 and May 31, 2017 — classified as 1 injury.

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

5 other recalls cover devices cleared under the same FDA submission (K902783); 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

  • Headache1
  • Malaise1
  • 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.

  • InjuryMay 31, 2017Occlusion Within Device; Occlusion Within Device

    IT WAS REPORTED TO MEDTRONIC NEUROSURGERY THAT THE PATIENT COMPLAINED ABOUT HEADACHES, FEELING OF PRESSURE ON THE HEAD, AND MALAISE. ACCORDING TO THE REPORT, THE SURGEON PRESUMED THAT THE DEVICE MAYBE OBSTRUCTED. REPORTEDLY, THE DEVICE WAS PARTIALLY EXPLANTED, AND THE PATIENT EXPERIENCED NO INJURIES.

    Patient problems: Headache; Malaise; Therapeutic Response, Decreased

    MAUDE report 6603289 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K902783. One submission often covers many models, so check the product and lot details in each record.

  • Z-1115-2021 · Jan 11, 2021 · Open, Classified
    Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for the following CFNs/REF numbers: 24048 - VALVE 24048 DELTA RGL PL 0.5, 24053 - CHAMBER 24053 DELTA, 24147 -
  • Z-0872-2021 · Dec 16, 2020 · Open, Classified
    REF 27219-2 X1, Medtronic, Delta Valve, Neonatal, Performance Level 2.0, CE 0344, Sterile EO - Product Usage: Neonatal Delta Snap Shunt Assemblies are components of CSF-Flow Contr
  • Z-0871-2021 · Dec 16, 2020 · Open, Classified
    REF 27219-1 X1, Medtronic, Delta Valve, Neonatal, Performance Level 1.0, CE 0344, Sterile EO - Product Usage: Neonatal Delta Snap Shunt Assemblies are components of CSF-Flow Contr
  • Z-0873-2021 · Dec 16, 2020 · Open, Classified
    REF 27219-5 X1, Medtronic, Delta Valve, Neonatal, Performance Level 1.5, CE 0344, Sterile EO - Product Usage: Neonatal Delta Snap Shunt Assemblies are components of CSF-Flow Contr
  • Z-0398-2014 · Nov 18, 2013 · Terminated
    Medtronic Delta Shunt Assembly Kit with Bioglide Small, Performance Level 1.0, Catalog No. 276201. Delta Shunt Assemblies are designed for use in shunting CSF from the lateral ve

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Sources and updates

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