CODMAN MEDOS 82-3041Recalls & reported problems
Cerenovus, Inc. · CODMAN MEDOS Ventricular Catheter Straight · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886704041252), received between Apr 6, 2022 and Aug 11, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Obstruction of Flow” (1 report).
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
- Adverse Event Without Identified Device or Use Problem1
- Obstruction of Flow1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 11, 2022Obstruction of Flow; Obstruction of Flow
A PHYSICIAN REPORTED A HAKIM VENTRICULAR CATHETER (ID 823041) WAS IMPLANTED TOGETHER WITH A CERTAS VALVE VIA V-P SHUNT ON UNKNOWN DATE WITH UNKNOWN SETTING. THE VENTRICULAR CATHETER WAS OBSTRUCTED THEREFORE THE CATHETER WAS REMOVED AND REPLACED ON (B)(6) 2022. THE CERTAS VALVE REMAINS IMPLANTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15211096 ↗InjuryApr 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
2 OF 2 REPORTS. OTHER MFG REPORT NUMBER: 3013886523-2022-00091. A PHYSICIAN REPORTED A CERTAS VALVE WAS IMPLANTED VIA V-P SHUNT ON UNKNOWN DATE WITH UNKNOWN SETTING. VALVE OBSTRUCTION WAS SUSPECTED AND ON (B)(6) 2022, THE VALVE AND THE VENTRICULAR CATHETER WERE REMOVED AND REPLACED.
Patient problems: Insufficient Information
MAUDE report 14021548 ↗
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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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