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Bemis 3004Recalls & reported problems

Bemis de México, S.A. de C.V. · 3000CC QUICKFIT LINER 50 PACK INDIVIDUALLY BAGGED · Class 2

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 10073088149548), received between Jan 18, 2019 and Jan 18, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Leak/Splash” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Leak/Splash1

Patient problems

  • 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.

  • MalfunctionJan 18, 2019Leak/Splash; Leak/Splash

    FACILITY REPORTS DIFFICULTY PUTTING FLEXIBLE LINERS ON HARD CANISTERS. WHEN VACUUM IS ON THEY SEAT, BUT WHEN VACUUM IS TURNED OFF THEY POP OFF. FACILITY REPORTS PHYSICIAN WAS SPLASHED WITH FLUID FROM CANISTER.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8262358 ↗

Other Apparatus, Suction, Operating-Room, Wall Vacuum Powered devices

All Apparatus, Suction, Operating-Room, Wall Vacuum Powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.