BD Sharps Collector 305435Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 2GAL RED · 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 00382903054350), received between Jul 3, 2018 and Jul 20, 2021 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Component Missing” (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
- Component Missing1
- Incorrect Device Or Component Shipped1
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 20, 2021Component Missing; Component Missing
IT WAS REPORTED THAT THE LIDS ARE MISSING WITH 15 BD SHARPS COLLECTOR. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED BY THE SALES REPRESENTATIVE THAT THE LIDS ARE MISSING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12197288 ↗MalfunctionMar 23, 2020Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE LID WAS MISSING WITH A BD SHARPS COLL 2GAL RED. THIS OCCURRED WITH 6 CONTAINERS AND AS DISCOVERED PRIOR TO USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED THAT SIX LIDS WERE MISSING WHEN THE SHIPMENT WAS RECEIVED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9868126 ↗MalfunctionJul 3, 2018Incorrect Device Or Component Shipped
IT WAS REPORTED THAT 3 CASES OF BD RECYKLEEN¿ SHARPS COLLECTORS WERE FOUND PACKAGED WITH THE "WRONG COVERS" PRIOR TO USE. THERE WAS NO REPORT OF EXPOSURE, SERIOUS INJURY OR MEDICAL INTERVENTION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7659471 ↗
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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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