BD Sharps Collector 305444Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL SIDE ENTRY 5.4QT PEARL 20/PK · Class 2
All models of BD Sharps Collector (34)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00382903054442), received between Feb 27, 2019 and Oct 6, 2022 — classified as 4 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
- Disconnection1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 6, 2022Component Missing; Component Missing
IT WAS REPORTED WHILE USING BD SHARPS COLL SIDE ENTRY 5.4QT PEARL 20/PK THE LID WAS MISSING. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MDS-BD1 VERBATIM: WE WERE NOTIFIED THAT ITEM BF305444'S LID IS MISSING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15557523 ↗MalfunctionOct 5, 2022Component Missing; Component Missing
IT WAS REPORTED THAT THE BD¿ PEARL SIDE ENTRY PATIENT ROOM COLLECTOR EXPERIENCED A MISSING LID. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER REPORTED MISSING LID.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15546532 ↗MalfunctionAug 12, 2019Component Missing; Component Missing
IT WAS REPORTED THAT THE LIDS RECEIVED WITH THE BD¿ PEARL SIDE ENTRY PATIENT ROOM COLLECTORS WERE THE WRONG SIZE, AND NOTICED BEFORE USE. THE CUSTOMER REPORTED 20 OCCURRENCES OF THIS EVENT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "WRONG LIDS"
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8883779 ↗MalfunctionFeb 27, 2019Disconnection
IT WAS REPORTED THAT THE SLIDING PART ON A SHARPS COLL SIDE ENTRY 5.4QT PEARL WAS NOT CONNECTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8374274 ↗
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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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