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Medline Industries, Inc. DYNDF1117Recalls & reported problems

Medline Industries, Inc. · CARILION CIRCUMCISION KIT · 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 10884389797884), received between Jun 15, 2018 and Jun 15, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Scratched Material” (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

  • Scratched Material1

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.

  • MalfunctionJun 15, 2018Scratched Material

    THE TIP OF THE HEMOSTAT IN THE CIRCUMCISION KIT WAS EXTREMELY SHARP AND WOULD HAVE PIERCED THE PATIENT'S PENIS HAD IT BEEN USED. THIS HAS OCCURRED ON SEVERAL OCCASIONS AND REQUIRES THE PHYSICIANS TO RETRIEVE ANOTHER HEMOSTAT. SOME OF THE HEMOSTATS ARE MORE BLUNT THAN OTHERS.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7605228 ↗

Other laparoscopy kit devices

All laparoscopy kit devices →

Sources and updates

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