BD Sharps Collector 305493Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL CHEMO 5GAL YEL CAP NON-VENT · 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 00382903054930), received between May 22, 2018 and Jan 26, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Puncture/Hole” (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
- Material Puncture/Hole1
- Missing Information1
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.
MalfunctionJan 26, 2023Missing Information; Missing Information
IT WAS REPORTED THAT THE HAZARD LABEL WAS MISSING ON THE BD¿ CHEMOTHERAPY SHARPS COLLECTOR. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "WE GOT ONE OF OUR SHARPS CONTAINERS WITH NO LABELING ON THE OUTSIDE. TYPICALLY THEY HAVE LIKE A HAZARDOUS LABEL AND WHAT NOT. THIS ONE CAME NAKED."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16251080 ↗MalfunctionMay 22, 2018Material Puncture/Hole
IT WAS REPORTED THAT THE BD CHEMO ONE-PIECE SHARPS COLLECTOR WITH PLUG CAP WAS REMOVED FROM A NEW BOX AND HAD A PUNCTURE ON THE BOTTOM. NO REPORTS OF SERIOUS INJUY OR MEDICAL INTERVENTION NOTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7531631 ↗
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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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