BD Sharps Collector 305601Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 9GAL 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
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00382903056019), received between Jun 17, 2019 and Sep 20, 2023 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Component Missing” (6 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 Missing6
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Known Impact Or Consequence To Patient2
- Insufficient Information1
- No Patient Involvement1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 20, 2023Component Missing; Component Missing
IT WAS REPORTED THAT THE34L BD¿ LARGE SHARPS COLLECTOR WERE MISSING LIDS. THE FOLLOWING WAS RECEIVED BY THE INITIAL REPORTER: INJURIES OR ADVERSE EVENT: NO REPORTED ISSUE: CUSTOMER RECEIVED SEALED BOX - NO LIDS, ONLY CONTAINERS. NO DAMAGE TOBOX.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17786265 ↗MalfunctionJun 9, 2023Component Missing; Component Missing
IT WAS REPORTED 8 SHARPS COLL 9GAL GASKET RED EXPERIENCED MISSING LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: INJURIES OR ADVERSE EVENT: NO REPORTED ISSUE: CUSTOMER XXXXXX TO REPORT QULITY ISSUE -THE CASE DID NOT HAVE ANY LIDS.
Patient problems: Insufficient Information
MAUDE report 17095592 ↗MalfunctionMar 3, 2021Component Missing; Component Missing
IT WAS REPORTED THAT 8 SHARPS COLL 9GAL GASKET RED EXPERIENCED MISSING LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 305601 FOR 8 EACH OF THE MISSING LIDS, QUANTITY 8 EACH , ISSUE WITH LID ¿ (EXAMPLE: MISSING LID, CRACKED, BROKEN).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11403038 ↗MalfunctionNov 6, 2020Component Missing; Component Missing
IT WAS REPORTED THAT THE SHARPS COLL 9GAL GASKET RED WAS RECEIVED WITHOUT A LID. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "REPORTED ISSUE: CUSTOMER RECEIVED BOX, UNOPENED AND NOT DAMAGED WITHOUT LIDS."
Patient problems: No Patient Involvement
MAUDE report 10805111 ↗MalfunctionAug 19, 2019Component Missing; Component Missing
IT WAS REPORTED THAT THE SHARPS COLL 9GAL GASKET RED EXPERIENCED A MISSING LID OR SLIDE CLAMP WHICH WAS NOTED PRIOR TO USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 305601, BATCH NO. 9033926. IT WAS REPORTED THE LID WAS MISSING.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8906265 ↗MalfunctionJun 17, 2019Component Missing; Component Missing
MATERIAL NO. 305601, BATCH NO. 9033926. IT WAS REPORTED THAT BEFORE USE OF THE SHARPS COLL 9GAL GASKET RED SHARPS CONTAINERS WERE MISSING LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: REPORTED A DEFECTIVE SHARPS CONTAINERS ON 5/9 AND WAS ADVISED THAT A REPLACEMENT WOULD BE SHIPPED TO OUR CUSTOMER. THE LOT NUMBER IS 9033926 AND THE CUSTOMER WAS MISSING THE LIDS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8703658 ↗
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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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