Skip to content

Delta® 42812 (UDI 00643169073784)Recalls & reported problems

Medtronic Ps Medical, Inc. · VALVE 42812 DELTA SMALL LEVEL I · 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 00643169073784), received between Aug 29, 2022 and Aug 29, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Infusion or Flow Problem” (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

  • Infusion or Flow Problem1

Patient problems

  • Unspecified Tissue Injury1

Recent adverse event reports

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

  • InjuryAug 29, 2022Infusion or Flow Problem; Infusion or Flow Problem

    MEDTRONIC RECEIVED INFORMATION REGARDING A DELTA VALUE DEVICE. IT WAS REPORTED THAT ON (B)(6) 2013 A VALVE WAS IMPLANTED. THE VALVE WAS NOT WORKING PROPERLY SO THE DEVICE WAS EXPLANTED (B)(6) 2022. THE VALVE WAS REPLACED WITH A DIFFERENT MANUFACTURERS PRODUCT. THERE WAS NO REPORTED ISSUES WITH THE PATIENT.

    Patient problems: Unspecified Tissue Injury

    MAUDE report 15313378 ↗

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

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