BD Sharps Collector 305666Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 19GAL GASKET RED · Class 2
All models of BD Sharps Collector (34)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00382903056668), received between Aug 27, 2019 and Jul 20, 2023 — classified as 7 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.
Most reported problems
Device problems
- Component Missing4
- Break1
- Device Misassembled During Manufacturing /Shipping1
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Known Impact Or Consequence To Patient3
- No Patient Involvement1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 20, 2023Component Missing; Component Missing
IT WAS REPORTED THAT 5 OF THE SHARPS COLL 19GAL GASKET RED WERE MISSING THEIR LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER REPORTED 5 RCVD THAT DID NOT INCLUDE THE LIDS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17358175 ↗MalfunctionAug 16, 2021Component Missing; Component Missing
IT WAS REPORTED THAT 2 CASES OF SHARPS COLL 19GAL GASKET RED WERE MISSING THEIR LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "THE LIDS ARE INTERCHANGEABLE AND AS MENTIONED PREVIOUSLY, WE RECEIVED #2 CASES WITHOUT LIDS. THIS EQUATES TO #10 CONTAINERS WITHOUT LIDS."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12329015 ↗MalfunctionJun 28, 2021Component Missing; Component Missing
IT WAS REPORTED THAT SHARPS COLL 19GAL GASKET RED LID WAS MISSING. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED BY THE DISTRIBUTOR THAT THE LIDS ARE MISSING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12079174 ↗MalfunctionJul 3, 2020Leak/Splash; Leak/Splash
IT WAS REPORTED THAT 5 SHARPS COLL 19GAL GASKET RED EXPERIENCED MISSING LIDS OR SLIDE LIDS/CLAMPS. PRODUCT DEFECT WAS NOTED PRIOR TO USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 305666 BATCH NO: 9158917 INJURIES OR ADVERSE EVENT: NO REPORTED ISSUE: LIDS ARE MISSING.
Patient problems: No Patient Involvement
MAUDE report 10228893 ↗MalfunctionFeb 19, 2020Break; Break
IT WAS REPORTED THAT THE LID ON THE SHARPS COLL 19GAL GASKET RED WOULD NOT CLOSE TIGHT AND LET GAS ESCAPE DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "PROBLEMATIC AT THE OPENING OF THIS CONTAINER WHICH LETS GAS ESCAPE SINCE IT DOES NOT CLOSE TIGHT".
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9728278 ↗MalfunctionJan 24, 2020Component Missing; Component Missing
IT WAS REPORTED THAT MISSING LIDS WERE FOUND BEFORE USE WITH A SHARPS COLL 19GAL GASKET RED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, "IT WAS REPORTED THAT THE LIDS WERE MISSING. EVENT DESCRIPTION PER ATTACHED EMAIL STATES: NO LIDS."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9628200 ↗MalfunctionAug 27, 2019Device Misassembled During Manufacturing /Shipping; Device Misassembled During Manufacturing /Shipping
IT WAS REPORTED THAT 19GAL RED BD¿ EXTRA LARGE SHARPS COLLECTOR WITH CLEAR SLIDE TOP WITH GASKET LIDS WERE BROKEN. THIS OCCURRED ON 3 OCCASIONS BEFORE USE. NO DATE/TIME OR PATIENT INFORMATION WAS GIVEN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 305666 BATCH, NO: UNKNOWN. IT WAS REPORTED THAT CUSTOMER RECEIVED 3 BROKEN LIDS. DESCRIPTION: RECEIVED A CALL STATING THAT HIS CUSTOMER RECEIVED THREE LIDS BROKEN LIDS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8935157 ↗
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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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