Skip to content

Medline Industries, Inc. DYNJ68770Recalls & reported problems

Medline Industries, Inc. · LAP BASIC GENERAL SURGERY · 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 10193489837919), received between Aug 17, 2021 and Aug 17, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Device” (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

  • Defective Device1

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.

  • MalfunctionAug 17, 2021Defective Device

    IT WAS REPORTED, LAP SPONGE IN A STERILE CUSTOM PACK IS DISCOVERED DIRTY AFTER THE PROCEDURE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12333486 ↗

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