Skip to content

Medline Industries, Inc. DYNJ54000BRecalls & reported problems

Medline Industries, Inc. · BUTLER LAPAROSCOPIC PACK · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942704903), received between Jun 21, 2018 and Jun 21, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Component Falling” (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 Falling1
  • Detachment Of Device Component1

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.

  • InjuryJun 21, 2018Detachment Of Device Component; Component Falling

    IT WAS REPORTED THAT DURING AN UNIDENTIFIED "BACK" PROCEDURE THE BLADE FELL OFF OF THE HANDLE AND INTO THE SURGICAL SITE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7624625 ↗

Other laparoscopy kit devices

All laparoscopy kit devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page