BD Sharps Collector 305610Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 17GAL RED · 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 00382903056101), received between Jan 8, 2020 and Oct 9, 2023 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Component Missing” (4 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.
Reports received per month
Most reported problems
Device problems
- Component Missing4
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Known Impact Or Consequence To Patient1
- No Patient Involvement1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 9, 2023Component Missing; Component Missing
IT WAS REPORTED WHILE USING BD SHARPS COLL 17GAL RED THE LIDS WERE MISSING. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: QUANTITY AFFECTED: 1 CASE. SERIAL/LOT NUMBER: (B)(6). PO: (B)(4). ARE ANY SAMPLES AVAILABLE FOR RETURN?: YES. REPORTED ISSUE: NO LIDS. CUSTOMER DISPOSITION REQUEST: REPLACEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17896176 ↗MalfunctionJul 22, 2021Component Missing; Component Missing
IT WAS REPORTED THAT 1 CASE OF 17 GAL BD¿ SHARPS COLLECTOR WAS RECEIVED WITH MISSING LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED BY THE FACILITY REPRESENTATIVE THAT THE CONTAINER IS MISSING LIDS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12211035 ↗MalfunctionJun 25, 2020Component Missing; Component Missing
IT WAS REPORTED THAT AN UNSPECIFIED NUMBER OF SHARPS COLL 17GAL RED EXPERIENCED THE LID OR SLIDE LID/CLAMP MISSING. PRODUCT DEFECT WAS NOTED PRIOR TO USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 305610 BATCH NO: 0044914 CUSTOMER SAYS ONE OF THE CASES IS MISSING ALL THE LIDS. WOULD LIKE THE LIDS SENT OUT.
Patient problems: No Patient Involvement
MAUDE report 10196825 ↗MalfunctionJan 8, 2020Component Missing; Component Missing
IT WAS REPORTED THAT MISSING LIDS WERE FOUND WITH A SHARPS COLL 17GAL RED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, "CONTAINERS CAME IN A BOX WITH NO LIDS - BOX HAD NOT BEEN OPENED AND RETAPED. THE BOX THAT THEY CAME IN WAS ALREADY OPENED WHEN WE GOT IT . IT WAS NOT RETAPED. I SENT A PACKING SLIP THAT CAME FROM THE BOX. THERE WOULD BE NO USE FOR THE SHARPS CONTAINERS WITHOUT THE TOP. SO NOW WE ARE STUCK WITH 5 SHARPS CONTAINERS WITH NO LIDS. THE LOT # IS 9078903 SOMEONE ACTUALLY PUT UP THE CONTAINERS THINKING THE LIDS HAD ALREADY BEEN TAKEN OUT. THEY HAD NOT. WE HAVE SEVERAL THAT EMPTY SUPPLIES. NO ONE TOOK THEM FROM THE BOX. WE HAVE NEVER HAD THIS ISSUE BEFORE. PLEASE RESOLVE."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9566353 ↗
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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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