Skip to content

Medline Industries, Inc. DYNJ44989FRecalls & reported problems

Medline Industries, Inc. · MINOR PROCEDURE 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 10889942547753), received between Nov 2, 2017 and Nov 2, 2017 — classified as 1 injury.

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

  • Material Disintegration1

Patient problems

  • Foreign Body In Patient1
  • 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.

  • InjuryNov 2, 2017Material Disintegration

    THE FACILITY REPORTED THAT THE GAUZE CAME APART TODAY WHILE IN THE PATIENT.

    Patient problems: Foreign Body In Patient; No Known Impact Or Consequence To Patient

    MAUDE report 6995956 ↗

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