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BD Oral Syringe 305209Recalls & reported problems

Becton, Dickinson And Company · SYRINGE ORAL 10ML AMBER · Class 1

All models of BD Oral Syringe (7)

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

Adverse event reports
6
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 30382903052098), received between Apr 5, 2022 and Jul 10, 2024 — classified as 1 injury, 5 malfunctions.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (1 report).

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: 0 reportsDec 2023: 2 reportsJan 2024: 2 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 1 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: 0 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 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Device Contamination with Chemical or Other Material1
  • Device Markings/Labelling Problem1
  • Disconnection1
  • Manufacturing, Packaging or Shipping Problem1
  • Missing Information1
  • Volume Accuracy Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions6

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 10, 2024Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

    POST INVESTIGATION FINDINGS REVEALED THAT THE FOREIGN MATTER WAS ACTUALLY SILICONE VISIBLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19716469 ↗
  • MalfunctionJan 22, 2024Volume Accuracy Problem; Volume Accuracy Problem

    IT WAS REPORTED THAT THE BD ORAL SYRINGE HAD A SCALE MARKING ISSUE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "WIFE IS A PEDIATRIC NURSE AT (B)(6) HOSPITAL AND IN PASSING MENTIONED SUBSTITUTING BAXTER ORAL SYRINGES FOR BD ORAL SYRINGES. IN DOING SO SHE ADVISED THE STAFF FEEL THE QUALITY OF THE BD SYRINGES IS NOT ADEQUATE FOR USE IN VARIOUS FUNCTIONS. THE STAFF HAS BEEN INSTRUCTED NOT TO USE THE BD SYRINGES FOR VARIOUS ACTIVITIES LIKE PUSHING ORAL MEDICATION OR FEEDING VIA TUBES AS THEY SLIP OFF THE TUBES. THE GRADUATIONS ON THE OUTSIDE OF THE SYRINGE ALSO WIPE OFF EASILY WHILE THE BAXTER CANNOT EVEN BE SCRATCHED OFF. THIS MEANS THE HCP'S DO NOT HAVE AN ACCURATE MEASUREMENT OF THE LIQUID IN THE SYRINGE. HCP'S CANNOT USE BD SYRINGES FOR A VARIETY OF ACTIVITIES." ITEM#305209

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18558564 ↗
  • MalfunctionJan 22, 2024Disconnection; Disconnection

    MATERIAL #: 305209, BATCH#: UNKNOWN. IT WAS REPORTED BY CUSTOMER THAT WIFE IS A PEDIATRIC NURSE AT HELEN DEVOS AND IN PASSING MENTIONED SUBSTITUTING BAXTER ORAL SYRINGES FOR BD ORAL SYRINGES. IN DOING SO SHE ADVISED THE STAFF FEEL THE QUALITY OF THE BD SYRINGES IS NOT ADEQUATE FOR USE IN VARIOUS FUNCTIONS. THE STAFF HAS BEEN INSTRUCTED NOT TO USE THE BD SYRINGES FOR VARIOUS ACTIVITIES LIKE PUSHING ORAL MEDICATION OR FEEDING VIA TUBES AS THEY SLIP OFF THE TUBES. THE GRADUATIONS ON THE OUTSIDE OF THE SYRINGE ALSO WIPE OFF EASILY WHILE THE BAXTER CANNOT EVEN BE SCRATCHED OFF. THIS MEANS THE HCP'S DO NOT HAVE AN ACCURATE MEASUREMENT OF THE LIQUID IN THE SYRINGE. HCPS CANNOT USE BD SYRINGES FOR A VARIETY OF ACTIVITIES. ITEM#305209. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. WIFE IS A PEDIATRIC NURSE AT HELEN DEVOS AND IN PASSING MENTIONED SUBSTITUTING BAXTER ORAL SYRINGES FOR BD ORAL SYRINGES. IN DOING SO SHE ADVISED THE STAFF FEEL THE QUALITY OF THE BD SYRINGES IS NOT ADEQUATE FOR USE IN VARIOUS FUNCTIONS. THE STAFF HAS BEEN INSTRUCTED NOT TO USE THE BD SYRINGES FOR VARIOUS ACTIVITIES LIKE PUSHING ORAL MEDICATION OR FEEDING VIA TUBES AS THEY SLIP OFF THE TUBES. TH

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18558506 ↗
  • MalfunctionDec 12, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem

    RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. THE EXPIRY DATE IS NOT MENTIONED ON THE BAG WITH SYRINGES OR ON THE SMALL BAG WITH CAPS LOT#: 0148085.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18312447 ↗
  • MalfunctionDec 7, 2023Missing Information; Missing Information

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18283411 ↗
  • InjuryApr 5, 2022Manufacturing, Packaging or Shipping Problem

    BD ORAL DISPENSING SYRINGES 10ML AMBER WITH TIP CAP LOT 0272366 HAS BOTH 5ML AND 10ML SYRINGES IN SOME OF THE PACKAGING AND ALL 5ML IN OTHER PACKAGES. FDA SAFETY REPORT ID# (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14021346 ↗

Other CONTAINER, LIQUID MEDICATION, GRADUATED devices

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Sources and updates

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