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LAPAROSCOPIC TUBING 2190Recalls & reported problems

Megadyne Medical Products, Inc. · Laparoscopic Tubing Set, Mega Vac Smoke Evacuator · 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 10614559102077), received between Jan 10, 2017 and Jan 10, 2017 — 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

  • Injury1

Recent adverse event reports

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

  • InjuryJan 10, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    PATIENT INJURY INVOLVING AN OPERATING ROOM FIRE.

    Patient problems: Injury

    MAUDE report 6239627 ↗

Other APPARATUS, EXHAUST, SURGICAL devices

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Sources and updates

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