BD Oral Syringe 305219Recalls & reported problems
Becton, Dickinson And Company · SYRINGE ORAL 10ML CLEAR · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30382903052197), received between Jun 1, 2026 and Jun 1, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Contamination /Decontamination Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 1, 2026Contamination /Decontamination Problem
IT WAS REPORTED THAT BD SYRINGE ORAL 10ML CLEAR CONTAINED FOREIGN MATTER. VERBATIM: COMPLAINT VIA PHONE. PIR ATTACHED. CASE DESCRIPTION: A CUSTOMER REPORTED THE PRESENCE OF AN OILY SUBSTANCE IN THE PLUNGER AREA, SPECIFICALLY AT THE TIP OF THE SYRINGE. THIS ISSUE HAS BEEN OBSERVED IN APPROXIMATELY 300 UNITS, AFFECTING BOTH THE 5ML AND 10ML ORAL SYRINGES. THE CUSTOMER EXPRESSED UNCERTAINTY ABOUT WHETHER THIS CONDITION IS NORMAL OR EXPECTED. PRODUCT: 10 ML BD CLEAR ORAL SYRINGE / 5 ML BD CLEAR ORAL SYRINGE REF#: 205219 10ML / 305218 5ML LOT#: 6022380 / 5094919
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25356436 ↗
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- BD Oral Syringe 305209Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED6 reports
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- BD Oral Syringe 305220Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED4 reports
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- BD Luer-Lok Female Cap 408531Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED3 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.