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CODMAN MEDOS 82-3048Recalls & reported problems

Cerenovus, Inc. · CODMAN MEDOS Straight Connector · Class 2 · Implant

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 10886704041283), received between May 28, 2021 and May 28, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Labelling, Instructions for Use or Training Problem” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Labelling, Instructions for Use or Training Problem1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionMay 28, 2021Labelling, Instructions for Use or Training Problem

    1 OF 2 REPORTS. OTHER MFG REPORT NUMBER: 3013886523-2021-00235. A FACILITY REPORTED THE INSTRUCTIONS FOR USE FOR THE HAKIM CONNECTORS HAS DIFFERENT DRAWINGS DIMENSIONS FOR SKU 823048 AND 823049. NO PATIENT CONTACT/INJURY REPORTED AND THE EVENT DID NOT LED TO SURGICAL DELAY.

    Patient problems: Insufficient Information

    MAUDE report 11900448 ↗

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.