CODMAN MEDOS 82-3049Recalls & reported problems
Cerenovus, Inc. · CODMAN MEDOS Right Angle Connector · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 10886704064909), 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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
2 OF 2 REPORTS. OTHER MFG REPORT NUMBER: 3013886523-2021-00234. 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 11900432 ↗
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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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