BD Sharps Collector 305490Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 8.2QT RED VENTED 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 00382903054909), received between Sep 27, 2019 and Oct 10, 2019 — 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
- Device Misassembled During Manufacturing /Shipping1
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 10, 2019Break; Break
IT WAS REPORTED THAT THE SHARPS COLL 8.2QT RED VENTED CAP EXPERIENCED A PERMANENT LID LOCK, AND DIFFICULT ASSEMBLY -LID DOES NOT FIT COLLECTOR. PRODUCT DEFECTS WERE NOTED PRIOR TO USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 305490, BATCH NO: UNKNOWN. PER CUSTOMER EMAIL: I NEED DIRECTIONS ON HOW TO PROPERLY DISPOSE OF ONE OF YOUR SHARPS CONTAINERS THAT HAS A MANUFACTURING ERROR. THE LID ON THIS CONTAINER WAS CUT OFF TOO SHORT AND IS MISSING THE PLASTIC PART THAT SEALS/LOCKS THE CONTAINER. WE HAVE NOT USED THE CONTAINER OR PUT ANY SHARPS INSIDE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9175223 ↗MalfunctionSep 27, 2019Device Misassembled During Manufacturing /Shipping; Device Misassembled During Manufacturing /Shipping
MATERIAL NO.: 305490. BATCH NO.: 8338003. IT WAS REPORTED THAT BEFORE USE OF THE SHARPS COLL 8.2QT RED VENTED CAP THE LID OF THE SHARPS CONTAINER WAS DISCOVERED BROKEN IN BOX.. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: LID OF SHARPS CONTAINER BROKEN WHEN PACKAGE WAS OPENED. NO DAMAGE TO OUTSIDE OF BOX OR OTHER PRODUCTS INSIDE BOX.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9129650 ↗
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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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