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CODMAN 82-1739Recalls & reported problems

Cerenovus, Inc. · CODMAN EVD 1.9mm I.D. Catheter Set Includes 35cm Ventricular Catheter, Stylet, Connector, Cap, Catheter Anchoring Clip and Trocar · Class 2

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 10886704040965), received between Jan 29, 2019 and Jan 29, 2019 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Air Embolism1

Recent adverse event reports

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

  • InjuryJan 29, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    AIR FOUND IN PATIENT'S VENTRICLES AFTER INSERTING EVD CATHETER.

    Patient problems: Air Embolism

    MAUDE report 8287527 ↗

Other Shunt, central nervous system and components devices

All Shunt, central nervous system and components devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.