Interlink 303405Recalls & reported problems
Becton, Dickinson And Company · 10ml Syringe Luer Lock Tip with Vial Access Cannula · Class 2
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00382903034055), received between Dec 15, 2017 and Nov 5, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Break” (4 reports).
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
- Break4
- Device Contamination with Chemical or Other Material1
Patient problems
- Injury2
- Needle Stick/Puncture1
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 5, 2025Break; Break
NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Needle Stick/Puncture
MAUDE report 23481189 ↗MalfunctionNov 5, 2025Break; Break
IT WAS REPORTED THAT THE BD SYRINGE 10ML LL W/INTERLINK VAC HAD TIP BREAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303405. BATCH # 5169514. VERBATIM: PHYSICIAN REPORTED THAT A BLUNT PLASTIC CANNULA BROKE AND STUCK HER WHILE ACCESSING A VIAL. SHE REPORTS THAT THIS IS THE SECOND INSTANCE OF THIS HAPPENING WITH THIS ITEM. ADDITIONAL INFORMATION PROVIDED: THIS IS THE SECOND TIME I HAVE EXPERIENCED A BREAK WITH THIS DEVICE. THE FIRST TIME WAS 1-2 YEARS AGO WHERE I WAS INJURED FROM THE PLASTIC BREAKING. AFTER THAT POINT, I HAVE ACTUALLY STOPPED USING THE PLASTIC PIECE. I TRADITIONALLY OPEN A SEPARATE BLUNT FILL NEEDLE FOR MY OWN SAFETY. THIS WEEK, I DID NOT HAVE THE BLUNT FILL NEEDLE READILY AVAILABLE AND NEEDED TO PROCEED WITH USING THE PLASTIC ONE PRE-PACKAGED WHERE I EXPERIENCED THE MALFUNCTION. FORTUNATELY, SKIN WAS NOT BROKEN THIS TIME. PREVIOUS EVENT I HAD A PUNCTURE TO MY HAND THAT REQUIRED ALTERATIONS TO SCRUBBING. I CANNOT FIND THE PHOTO THAT I SENT TO OR LEADERSHIP FROM THE PREVIOUS EVENT IN THE LAST COUPLE YEARS. THIS TIME WAS LAST MONDAY. FOR MORE DETAIL ON MY INJURY, I HAD A LACERATION THAT DID NOT REQUIRE SUTURING. I USED TOPICAL AGENTS
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23481187 ↗MalfunctionOct 19, 2018Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT BD¿ 10 ML SYRINGE WITH INTERLINK® VIAL ACCESS CONTAINED FOREIGN MATTER. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7986812 ↗MalfunctionDec 19, 2017Break
IT WAS REPORTED THAT THE TIPS ON BD" SYRINGES WITH INTERLINK¿ VIAL ACCESS ARE BREAKING IN VIALS. TWO NURSES RECEIVED SCRATCHES FROM THE BROKEN TIPS. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.
Patient problems: Injury
MAUDE report 7131984 ↗MalfunctionDec 15, 2017Break
IT WAS REPORTED THAT THE TIPS ON BD" 10 ML SYRINGES WITH INTERLINK¿ VIAL ACCESS BROKE IN VIALS. TWO NURSES RECEIVED SCRATCHES FROM THE BROKEN TIPS. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.
Patient problems: Injury
MAUDE report 7122577 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.