Interlink 303347Recalls & reported problems
Becton, Dickinson And Company · 5ml Syringe Luer Lock Tip with Blunt Plastic Cannula · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00382903033478), received between Nov 5, 2020 and Apr 5, 2023 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (2 reports).
2 other recalls cover devices cleared under the same FDA submission (K974363); they may or may not involve this specific model.
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
- Device Contamination with Chemical or Other Material2
- Device-Device Incompatibility1
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Patient Involvement1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 5, 2023Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT BLACK FOREIGN MATTER WAS FOUND ON THE BD LUER-LOK¿ TIP SYRINGE WITH BLUNT PLASTIC CANNULA. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "FOUND CONTAMINATED WITH A BLACK SUBSTANCE THAT LOOKED LIKE DROPS OF INK OR MOLD. IT WAS RECOGNIZED PRIOR TO USE ON THE PATIENT".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16683140 ↗MalfunctionSep 22, 2022Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE BD SYRINGE 5ML LL W/BLUNT PLASTIC CANNULA BROKE OFF IN VIAL.THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THIS IS A PICTURE OF THE PRODUCT THAT WE HAVE SEEN THE TIP BRAKE OFF OF SEVERAL TIMES IN VIALS OF MEDICATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15463923 ↗MalfunctionJun 2, 2022Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT 1 BD SYRINGE 5ML LL W/BLUNT PLASTIC CANNULA HAD CORING ISSUES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER : THE CONSUMER FACILITY REPORTED ISSUES WITH THE BLUNT PLASTIC CANNULAS THAT WHEN THE NURSING STAFF ARE USING THESE TO DRAW UP MEDICATIONS FROM A VIAL, THEY ARE PUSHING PART OF THE RUBBER STOPPER INTO THE BOTTLE. EVENT DATE : UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14578690 ↗MalfunctionNov 5, 2020Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD 10ML SYRINGE WITH LUER-LOK TIP WITH BLUNT PLASTIC CANNULA. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WHEN UNPACKING, THE HCP FOUND THAT THE TIP OF THE SYRINGE (BLUNT CANNULA/VIAL ACCESS COMPONENT) WAS DAMAGED.
Patient problems: No Patient Involvement
MAUDE report 10796068 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K974363. One submission often covers many models, so check the product and lot details in each record.
- Z-1055-2015 · Dec 19, 2014 · TerminatedBD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula, Not for Skin Injection ; Catalog #303348, BD 10 mL Syringe Luer-Lok Tip with Blunt Fill Needle 18G x 1 1/2 (1.2mm x 4
- Z-1461-06 · Jun 21, 2006 · TerminatedBD Vacutainer Blood Collection Assembly with BD Blunt Plastic Cannula; Catalog #303380.
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- N/A 305106Becton, Dickinson And Company · Needle, hypodermic, single lumen1 recall467 reports
- N/A 305110Becton, Dickinson And Company · Needle, hypodermic, single lumen418 reports
- BD Safe-Clip 328235Becton, Dickinson and Company Inc · Needle, hypodermic, single lumen268 reports
- BD Ultra-Fine 320109Becton Dickinson Pen Limited · Needle, hypodermic, single lumen229 reports
- BD AutoShield Duo 329515Becton, Dickinson And Company · Needle, hypodermic, single lumen208 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.