Bemis 1504RBM NRecalls & 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 10073088159530), received between May 7, 2022 and May 7, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (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
- Leak/Splash2
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 7, 2022Leak/Splash; Leak/Splash
CAREMOUNT MEDICAL P.C. HAD TWO MORE EVENTS OF THE BEMIS LINER 1504RBM N LEAKING SUCTIONED CONTENTS INTO THE OUTER HARD CANISTER. THIS REPORT IS FOR THE EVENT ON 4/5/22 LOT 202605.
Patient problems: Insufficient Information
MAUDE report 14316738 ↗MalfunctionMay 7, 2022Leak/Splash; Leak/Splash
CAREMOUNT MEDICAL P.C. HAD ANOTHER EVENT OF THE BEMIS LINER 1504RBM N LEAKING SUCTION CONTENTS INTO THE OUTER HARD CANISTER.
Patient problems: Insufficient Information
MAUDE report 14316336 ↗
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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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