BD Sharps Collector 305456Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 14QT RED 1103 NON-VENT CAP · 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 00382903054565), received between Sep 30, 2020 and Jun 19, 2023 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Device Misassembled During Manufacturing /Shipping” (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
- Device Misassembled During Manufacturing /Shipping3
- Material Deformation2
- Fracture1
- Manufacturing, Packaging or Shipping Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- 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.
MalfunctionJun 19, 2023Material Deformation; Material Deformation
IT WAS REPORTED THAT THE BD¿ MULTIUSE NESTABLE SHARPS COLLECTOR LID WAS DEFORMED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM JAPANESE TO ENGLISH: THIS IS A REPORT ABOUT A DEFORMED LID OF SHARPS COLLECTOR. ACCORDING TO THE CUSTOMER'S REPORT, THE SHAPE OF THE LID WAS FOUND TO BE DIFFERENT FROM THE USUAL ONE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17159652 ↗MalfunctionMay 18, 2023Manufacturing, Packaging or Shipping Problem; Material Deformation; Manufacturing, Packaging or Shipping Problem; Material Deformation
IT WAS REPORTED THAT THE BD¿ MULTIUSE NESTABLE SHARPS COLLECTOR LID WAS DEFORMED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THIS IS A REPORT ABOUT A DEFORMED LID OF SHARPS COLLECTOR. ACCORDING TO THE CUSTOMER'S REPORT THE SHAPE OF THE LID OF SHARPS COLLECTOR WAS DIFFERENT FROM THE USUAL ONE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16959276 ↗MalfunctionApr 14, 2023Device Misassembled During Manufacturing /Shipping; Device Misassembled During Manufacturing /Shipping
IT WAS REPORTED THAT 20 BD¿ MULTIUSE NESTABLE SHARPS COLLECTOR LID WAS DEFORMED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THIS IS A REPORT ABOUT A DEFORMED LID OF SHARPS COLLECTOR. ACCORDING TO THE CUSTOMER'S VERBATIM REPORT, THE SHAPE OF THE LID OF SHARPS COLLECTOR 13.2L WAS DIFFERENT FROM THE USUAL ONE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16747006 ↗MalfunctionJul 30, 2022Fracture; Fracture
IT WAS REPORTED THAT WHILE USING THE BD¿ MULTI-USE NESTABLE SHARPS COLLECTOR THERE WAS TEN CRACKS AND/OR DAMAGES ON LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM JAPANESE TO ENGLISH: THIS IS A REPORT ABOUT DAMAGED LIDS OF SHARPS COLLECTOR. DURING THE INSPECTION AT THE CUSTOMER'S SIDE, CRACKS AND/OR DAMAGES ON LIDS WERE FOUND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15136672 ↗MalfunctionSep 29, 2021Device Misassembled During Manufacturing /Shipping; Device Misassembled During Manufacturing /Shipping
IT WAS REPORTED THAT 9 SHARPS COLL 14QT RED 1103 NON-VENT CAP LIDS WERE DAMAGED/BROKEN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM (B)(6) TO ENGLISH: "THE CUSTOMER REPORTED THAT THE PRODUCT HAD ARRIVED WITH THE LID SHUT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12547114 ↗MalfunctionSep 30, 2020Device Misassembled During Manufacturing /Shipping; Device Misassembled During Manufacturing /Shipping
IT WAS REPORTED THAT THE SHARPS COLL 14QT RED 1103 NON-VENT CAP WAS BROKEN BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM JAPANESE TO ENGLISH: "THIS IS A REPORT ABOUT A LID ISSUE OF SHARPS CONTAINER (13.2L). ACCORDING TO THE CUSTOMER'S REPORT, THE ROUND PART OF THE LID WAS SEPARATED FROM THE CONTAINER."
Patient problems: No Patient Involvement
MAUDE report 10610832 ↗
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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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