Interlink 303403Recalls & reported problems
Becton, Dickinson And Company · 5ml Syringe Luer Lock Tip with Vial Access Cannula · Class 2
- 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 00382903034031), received between Jul 5, 2019 and Jul 5, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Leak/Splash” (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
- Leak/Splash1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 5, 2019Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD 5ML SYRINGE WITH LUER-LOK TIP WITH VIAL ACCESS CANNULA EXPERIENCED DIFFICULT PLUNGER MOVEMENT DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 303403 BATCH NO. 8057945 DOCTOR WAS TRYING TO DRAW UP MEDICATION AND WAS EXPERIENCING DIFFICULTY WHEN PULLING ON PLUNGER ROD.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8764533 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.