Interlink 303366Recalls & reported problems
Becton, Dickinson And Company · Syringe Cannula · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00382903033669), received between Nov 18, 2020 and Aug 16, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break1
- Defective Device1
- Leak/Splash1
Patient problems
- Insufficient Information1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 16, 2021Break; Defective Device; Break; Defective Device
IT WAS REPORTED THAT THE CANNULA INTERLINK SYRINGE WAS DEFECTIVE/DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "A0203 - DEFECTIVE DEVICE A0401 - BREAK."
Patient problems: Insufficient Information
MAUDE report 12328906 ↗MalfunctionNov 18, 2020Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE CANNULA INTERLINK SYRINGE TIP BROKE OFF DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "BD SYRINGE PLASTIC NEEDLE BROKE INSIDE IV INJECTION SITE OF IV BUROTHROL DID NOT FALL INSIDE THE SOLUSET & PT ABLE TO RECEIVE HIS MORPHINE IV. 1)TUBING PUMP SET CUSTOM W/3 (NOT READABLE) SPLIT SEPTUM INJECTION PORT CSR #83869 2)CANNULA SYRINGE W/TOP PORT BED CSR # 21903"
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10865126 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.