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Melker G04652Recalls & reported problems

Cook Incorporated · Melker Uncuffed Emergency Cricothyrotomy Catheter Set · Class 2

All models of Melker (6)

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 00827002046528), received between Mar 27, 2018 and Mar 27, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Dull, Blunt” (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

  • Dull, Blunt1

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.

  • MalfunctionMar 27, 2018Dull, Blunt

    THE COMPLAINANT REPORTED THAT THE SCALPEL PROVIDED IN THE MELKER EMERGENCY CRICOTHYROTOMY CATHETER SET WAS DULL AND UNUSABLE. THIS PRODUCT PROBLEM OCCURRED TWICE, BUT IT DID NOT RESULT IN ANY REPORTED ADVERSE EFFECTS TO THE PATIENTS.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7374280 ↗

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Sources and updates

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