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Medline Industries, Inc. DYNJ903234CRecalls & reported problems

Medline Industries, Inc. · GENERAL LAPAROSCOPY · 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 10195327187828), received between Dec 5, 2022 and Dec 5, 2022 — classified as 1 injury.

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

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • InjuryDec 5, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    ACCORDING TO THE FACILITY ON (B)(6) 2022 DURING A LAPAROSCOPIC PROCEDURE, 'THE RAYTEC GAUZE ARE BEING USED TO WIPE THE TROCAR SITES OUT AND LEAVING FIBERS IN THE SURGICAL SITE'.

    Patient problems: Foreign Body In Patient

    MAUDE report 15914849 ↗

Other laparoscopy kit devices

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Sources and updates

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