BD Sharps Collector 305464Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 14QT RED 1508 NON-VENT CAP · Class 2
All models of BD Sharps Collector (34)
Data updated Oct 18, 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 00382903054640), received between Apr 14, 2020 and Jun 30, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Break1
- Component Missing1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- 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.
MalfunctionJun 30, 2021Component Missing; Component Missing
IT WAS REPORTED THAT THE BD SHARPS COLLECTOR 14 QT MULTI-USE NESTABLE EXPERIENCED A MISSING LID. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WE HAVE A FEW CONTAINERS THAT DO NOT HAVE LIDS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12097474 ↗MalfunctionApr 14, 2020Break; Break
IT WAS REPORTED THAT ONE OF THE LID CORNERS WOULDN'T "SNAP ON TIGHT" TO THE SHARPS COLL 14QT RED 1508 NON-VENT CAP BEFORE USE, MAKING IT SO THE COVER CAME OFF "EASIER THAN USUAL". THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "IT SEEMS THAT ONE OF THE CORNERS DOES NOT SNAP ON TIGHT MAKING THE COVER COME OFF EASIER THAN USUAL. IN THE PAST, ONCE THEY WERE CLOSED IT WAS IMPOSSIBLE TO REOPEN THEM."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9956112 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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