BD Oral Syringe 305217Recalls & reported problems
Becton, Dickinson And Company · SYRINGE ORAL 1ML 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 30382903052173), received between Sep 29, 2023 and Sep 29, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective Component” (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.
Most reported problems
Device problems
- Defective Component1
- Physical Resistance/Sticking1
Patient problems
- Insufficient Information1
- 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.
MalfunctionSep 29, 2023Defective Component; Physical Resistance/Sticking; Defective Component; Physical Resistance/Sticking
IT WAS REPORTED THAT THE BD¿ ORAL DISPENSING SYRINGE HAD DIFFICULT PLUNGER MOVEMENT WHILE TRYING TO PUSH OUT MEDICATION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CAN DRAW - BUT IS TREMENDOUS FORCE TO GET ANY MEDICATION OUT. EVERY SINGLE ONE IN THE BOX - USED TO ALWAYS BE A FEW BUT SO FAR THIS WHOLE BOX IS THE SAME WAY. GOT HER BOX IN AUGUST 29TH BUT SHE HAS BEEN REUSING OTHER ONES FROM PERVIOUS ORDERS SINCE THESE DO NOT SEE TO BE WORKING."
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 17848897 ↗
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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.