BD Sharps Collector 305076Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL CHEMO 3GAL YELLOW NEW CAP · Class 2
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00382903050765), received between Feb 12, 2020 and Nov 7, 2022 — classified as 5 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Device Misassembled During Manufacturing /Shipping3
- Defective Component1
- Device Markings/Labelling Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Known Impact Or Consequence To Patient1
- No Patient Involvement1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 7, 2022Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED BY THE CUSTOMER THAT 18 BD SHARPS COLL CHEMO 3GAL YELLOW NEW CAP HAD INCORRECT LABEL INFORMATION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THEY ARE SUPPOSED TO BE VENDOR NUMBER: 305076 3 GALLON YELLOW, BUT THEY HAVE VENDOR NUMBER: 305489 6.9 QT RED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15749220 ↗MalfunctionJul 22, 2021Defective Component; Defective Component
IT WAS REPORTED THAT SHARPS COLL CHEMO 3GAL YELLOW NEW CAP HAD A DAMAGED LID. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: " DURING INSPECTION, THE CUSTOMER DISCOVERED THAT THE LID WAS DAMAGED AT THE JOINT AREA AND DETACHED."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12208119 ↗MalfunctionApr 26, 2021Device Misassembled During Manufacturing /Shipping; Device Misassembled During Manufacturing /Shipping
IT WAS REPORTED THAT SHARPS COLL CHEMO 3GAL YELLOW NEW CAP LID WAS DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THIS IS A REPORT ABOUT A DAMAGED LID OF SHARPS COLLECTOR. ACCORDING TO THE CUSTOMER'S REPORT, THE LID WAS FOUND TO BE DAMAGED UPON ARRIVAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11729275 ↗MalfunctionJan 18, 2021Device Misassembled During Manufacturing /Shipping; Device Misassembled During Manufacturing /Shipping
IT WAS REPORTED THAT SHARPS COLL CHEMO 3GAL YELLOW NEW CAP LID WAS DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: ACCORDING TO THE CUSTOMER'S REPORT, THE DUAL-OPENING TOP OF THE LID WAD DAMAGED AT ITS HINGE.
Patient problems: No Patient Involvement
MAUDE report 11190295 ↗MalfunctionFeb 12, 2020Device Misassembled During Manufacturing /Shipping; Device Misassembled During Manufacturing /Shipping
IT WAS REPORTED THAT SHARPS COLL CHEMO 3GAL YELLOW NEW CAP LID WAS DISCONNECTED. THIS WAS DISCOVERED BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WHEN THE CUSTOMER OPENED THE LID BEFORE USE, THE CONNECTION WAS DETACHED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9699952 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.