Skip to content

CODMAN 26-1223Recalls & reported problems

Cerenovus, Inc. · CODMAN Disposable Perforator 9mm · Class 2

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 10886704005124), received between Aug 3, 2018 and Aug 3, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Auto Stop” (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

  • Failure to Auto Stop1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionAug 3, 2018Failure to Auto Stop; Failure to Auto Stop

    AS REPORTED BY THE REP, A CODMAN PERFORATOR FAILED TO DISENGAGE AFTER DRILLING COMPLETELY THROUGH THE BONE. THERE WAS NO ADVERSE CONSEQUENCES TO THE PATIENT. NO DELAYS WERE REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7746764 ↗

Other DRILLS, BURRS, TREPHINES & ACCESSORIES (COMPOUND, POWERED) devices

All DRILLS, BURRS, TREPHINES & ACCESSORIES (COMPOUND, POWERED) devices →

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