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Medline Industries, Inc. DYNJ902535JRecalls & reported problems

Medline Industries, Inc. · CARDIAC - KORVER · Class 2

Data updated Oct 18, 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 10193489335101), received between Feb 22, 2021 and Feb 22, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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 18, 2026.

Most reported problems

Device problems

  • Component Missing1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionFeb 22, 2021Component Missing

    IT WAS REPORTED THAT THE CUSTOMER WAS UNDERGOING A CARDIAC PROCEDURE AND IN THE MIDDLE OF THE PROCEDURE THE TIP OF THE BLOWER WAS NOTED TO BE MISSING FROM THE DEVICE. IT IS UNKNOWN IF THE TIP BLEW OFF IN THE PATIENT OR OUTSIDE OF THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11361539 ↗

Other Cardiovascular procedure kit devices

All Cardiovascular procedure kit devices →

Sources and updates

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