Bemis 1504Recalls & reported problems
Bemis de México, S.A. de C.V. · 1500CC QUICKFIT LINER 50 PACK INDIVIDUALLY BAGGED · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10073088149210), received between Aug 27, 2019 and Sep 27, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (2 reports).
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
- Fluid/Blood Leak2
Patient problems
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 27, 2019Fluid/Blood Leak; Fluid/Blood Leak
CUSTOMER REPORTS THAT THEY HAD A SUCTION LINER WITH A TEAR IN IT AS THEY PREPARED TO REMOVE IT FROM THE CANISTER, ALLOWING FOR SUCTIONED CONTENTS TO SPILL INTO THE CANISTER.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9130827 ↗MalfunctionAug 27, 2019Fluid/Blood Leak; Fluid/Blood Leak
COMPLAINANT STATES THAT THEY HAVE EXPERIENCED SIX SUCTION LINERS 'BREAK FROM THE LID WHEN IN THE CANISTER.' THERE ARE NO PATIENT CONSEQUENCES, BUT THE CUSTOMER STATES THAT THEY AREN'T ABLE TO USE THE BEMIS QUICK DRAIN UNIT TO DISPOSE OF THE FLUID BECAUSE IT MIGHT EXPOSE STAFF TO POTENTIALLY INFECTIOUS WASTE. STAFF MUST USE ALTERNATE METHOD OF DISPOSAL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8935660 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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