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BD Sharps Collector 305603Recalls & reported problems

Becton, Dickinson And Company · SHARPS COLL CHEMO 9GAL YELLOW · Class 2

All models of BD Sharps Collector (34)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
8
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00382903056033), received between Jun 10, 2019 and Jun 3, 2025 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Component Missing” (7 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

Nov 2023: 1 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Component Missing7
  • Retraction Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions3
  • No Known Impact Or Consequence To Patient2
  • Insufficient Information1
  • No Information1
  • No Patient Involvement1

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 3, 2025Retraction Problem; Retraction Problem

    IT WAS REPORTED THAT BD INSYTE AUTOGUARD NEEDLE DID NOT RETRACT PULLING CATHETER WITH IT DURING PROCESS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: ATTEMPTING TO START THE PATIENT'S IV, IV WAS SUCCESSFULLY STARTED BUT WHEN ATTEMPTING TO RETRACT THE NEEDLE TO SPRING JAMMED AND DID NOT RETRACT THE NEEDLE OR ALLOW THE NEEDLE TO BE REMOVED FROM THE IV CATHETER. WHILE ATTEMPTING TO GET THE NEEDLE TO RETRACT THE IV CATHETER WAS PULLED OUT OF THE VEIN CAUSING THE PATIENT TO NEED ANOTHER IV ATTEMPT OTHER SERIOUS OR IMPORTANT MEDICAL EVENTS.

    Patient problems: Insufficient Information

    MAUDE report 22131350 ↗
  • MalfunctionNov 20, 2023Component Missing; Component Missing

    IT WAS REPORTED THAT BD SHARPS DISPOSAL LID WAS MISSING. THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE FOLLOWING VERBATIM: THE CUSTOMER ORDERED THE ITEM FROM MCKESSON THEY STATED THEY RECEIVED 1 CASE OF THE ITEM BUT WERE MISSING THE LIDS. I HAVE REACHED OUT TO THE PRODUCT COMPLAINT TEAM THEY CREATED A CASE#(B)(4). THEY INFORMED TO REACH OUT WITH THIS CASE NUMBER FOR REIMBURSEMENT FOR THE MISSING PART. SHARPS COLL CHEMO 9GAL YELLOW.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18179402 ↗
  • MalfunctionApr 28, 2022Component Missing; Component Missing

    IT WAS REPORTED BD¿ SHARPS COLL CHEMO 9GAL YELLOW WAS MISSING ITS LID. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "IT WAS REPORTED BY THE CONSUMER THE LIDS WERE MISSING."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14240258 ↗
  • MalfunctionJun 21, 2021Component Missing; Component Missing

    IT WAS REPORTED THAT SHARPS COLL CHEMO 9GAL YELLOW WAS MISSING LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED THAT THE CUSTOMER RECEIVED 1 CASE OF CONTAINERS WITHOUT LIDS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12038050 ↗
  • MalfunctionSep 1, 2020Component Missing; Component Missing

    IT WAS REPORTED THAT THE SHARPS COLL CHEMO 9GAL YELLOW WERE RECEIVED WITHOUT LIDS, WHICH WAS NOTICED PRIOR TO USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "THE ENTIRE CASE WAS MISSING LIDS. I THINK THE CASE WAS SOLD, THEN RETURNED WITHOUT LIDS, THEN SOLD AGAIN. IT LOOKED LIKE THE TOP OF THE CASE HAD BEEN OPENED AND RESEALED.".

    Patient problems: No Patient Involvement

    MAUDE report 10480666 ↗
  • MalfunctionJan 29, 2020Component Missing; Component Missing

    IT WAS REPORTED BY THE DISTRIBUTOR THAT THE CUSTOMER WAS MISSING THREE LIDS FOR BD SHARPS DISPOSAL CONTAINER MATERIAL NO.: 305603. BATCH NO.: UNKNOWN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: REPORTED BY THE THAT THE CUSTOMER WAS MISSING THREE LIDS.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9641016 ↗
  • MalfunctionJan 14, 2020Component Missing; Component Missing

    IT WAS REPORTED THAT 8 SHARPS COLL CHEMO 9GAL YELLOW 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: 305603 BATCH NO: 9257921. EVENT DESCRIPTION PER STATES: NO LIDS. PRODUCT WAS SHIPPED FROM DISTRIBUTOR TO THE CUSTOMER.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9589010 ↗
  • MalfunctionJun 10, 2019Component Missing; Component Missing

    IT WAS REPORTED THAT BD SHARPS¿ COLLECTOR CHEMOTHERAPY 9 GAL YELLOW CAME WITH NO LIDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO.: 305603 BATCH NO.: UNKNOWN. IT WAS REPORTED THAT NO LIDS WERE RECEIVED WITH THE SHARPS CONTAINER.

    Patient problems: No Information

    MAUDE report 8683866 ↗

Other Needle, hypodermic, single lumen devices

All Needle, hypodermic, single lumen devices →

Sources and updates

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