BD Sharps Collector 305422Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 2GAL PEARL · 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 00382903054220), received between Aug 2, 2019 and Sep 10, 2019 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Component Missing” (2 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 Missing2
- Break1
Patient problems
- No Known Impact Or Consequence To Patient3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 10, 2019Component Missing; Component Missing
IT WAS REPORTED THAT MIXED PRODUCT WAS FOUND BEFORE USE WITH A SHARPS COLL 2GAL PEARL. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, "IT WAS REPORTED THAT THREE CASES OF 2 GALLON SHARPS CONTAINERS ARRIVED WITH DIFFERENT LIDS. PER EMAIL: THE 2 GALLON SHARPS CONTAINERS HAVE ARRIVED WITH DIFFERENT LIDS, WHICH DO NOT FIT IN THE WALL CABINETS. SO, THEY ARE UNABLE TO USE THESE SHARPS CONTAINERS."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8983444 ↗MalfunctionAug 14, 2019Break; Break
IT WAS REPORTED THAT 10 SHARPS COLL 2GAL PEARL WERE RECEIVED WITH THE INCORRECT LIDS. THE DEFECT WAS NOTICED BEFORE USE. THIS COMPLAINT WAS CREATED TO CAPTURE THE 2ND OF 2 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "OK, SO I OPENED UP ANOTHER BOX OF SHARPS CONTAINERS TODAY WITH THE WRONG LIDS."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8894521 ↗MalfunctionAug 2, 2019Component Missing; Component Missing
MATERIAL NO: 305422, BATCH NO: 9112926. IT WAS REPORTED THAT BEFORE USE OF THE SHARPS COLL 2GAL PEARL THE SHARPS CONTAINERS WERE RECEIVED WITH THE INCORRECT LIDS. THERE WERE TEN SHARPS CONTAINERS THAT HAD THE WRONG LID. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "THE 305422 (2G SHARPS CONTAINERS) ARRIVE WITH DIFFERENT TOPS THAT DO NOT FIT THE BD WALL CABINETS."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8855250 ↗
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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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