BD Sharps Collector 305344Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 8QT NEST FUNL TOP NEEDL PORT · Class 2
All models of BD Sharps Collector (34)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382903053445), received between Nov 25, 2020 and Jun 27, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Component Missing” (3 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Component Missing3
- Device Misassembled During Manufacturing /Shipping1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 27, 2023Component Missing; Component Missing
IT WAS REPORTED THAT 3 BD 8QT SHARPS COLLECTOR HAD LIDS MISSING. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER REPORTED MISSING LIDS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17213750 ↗MalfunctionDec 6, 2022Component Missing; Component Missing
IT WAS REPORTED THAT 4 BD 8QT SHARPS COLLECTORS EXPERIENCED MISSING LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MISSING THE ALL FUNNEL TOPS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15927899 ↗MalfunctionNov 25, 2020Component Missing; Device Misassembled During Manufacturing /Shipping; Component Missing; Device Misassembled During Manufacturing /Shipping
IT WAS REPORTED THAT A SHARPS COLL 8QT NEST FUNL TOP NEEDL PORT WAS RECEIVED TWO UNITS WITH BROKEN LIDS AND TWO UNITS WITH MISSING LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: REPORTING THAT HE RECEIVED SHARP CONTAINERS WITH BROKEN LIDS (TWO OF THEM) AND ANOTHER TWO WERE MISSING.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; No Clinical Signs, Symptoms or Conditions
MAUDE report 10900901 ↗
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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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