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Medline Industries, Inc. DYNJ0365463GRecalls & reported problems

Medline Industries, Inc. · CLOSUREFAST PROCEDURE PACK-LF · 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 10889942059508), received between Oct 4, 2019 and Oct 4, 2019 — 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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Perforation of Vessels1

Recent adverse event reports

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

  • InjuryOct 4, 2019Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED, "EITHER THE TUMESCENT NEEDLES OR THE STAB PHLEBOTOMY (CARRIED OUT AFTER RF ABLATION) NICKED THE ARTERY."

    Patient problems: Perforation of Vessels

    MAUDE report 9156136 ↗

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Sources and updates

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