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Interlink 303348Recalls & reported problems

Becton, Dickinson And Company · 10ml Syringe Luer Lock Tip with Blunt Plastic 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 00382903033485), received between Dec 15, 2017 and Dec 13, 2025 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Contamination” (1 report).

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 1 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Contamination1
  • Contamination /Decontamination Problem1
  • Device Contamination with Chemical or Other Material1
  • Dull, Blunt1
  • Packaging Problem1
  • Structural Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions4
  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 13, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

    IT WAS REPORTED THAT THE BD SYRINGE 10ML LL W/BLUNT PLASTIC CANN HAD FOREIGN MATTER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303348 LOT # 5169511 VERBATIM: RCC RECEIVED A COMPLAINT VIA COMMUNITY. PIR ATTACHED. WHEN USED TO DRAW MEDICATION, BLACK ITEMS WILL BE IN THE MEDICATION SYRINGE. ¿ PRODUCT CODE: 303348 PATIENT/HCP IMPACT: WASTING OF MEDICATIONS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23798682 ↗
  • MalfunctionJul 13, 2022Contamination; Contamination

    IT WAS REPORTED WHILE USING BD INTERLINK¿ 10 ML SYRINGE WITH BLUNT PLASTIC CANNULA CORING OCCURRED. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED BY CUSTOMER THAT AFTER THE MEDICATION VIAL WAS PUNCTURED WITH THE SYRINGE THE VIAL WAS NOTED TO HAVE RETAINED SHARDS OF THE RUBBER STOPPER FROM THE TOP OF THE VIAL. AFTER THE MEDICATION VIAL WAS PUNCTURED WITH THE SYRINGE, THE VIAL WAS NOTED TO HAVE RETAINED SHARDS OF THE RUBBER STOPPER FROM THE TOP OF THE VIAL.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15004562 ↗
  • MalfunctionJun 2, 2022Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

    IT WAS REPORTED THAT 1 BD CANNULA WITH SYRINGE INTERLINK® BLUNT TIP 10 ML HAD FOREIGN MATTER IN THE FLUID PATH. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER : THE CONSUMER REPORTED HAVING SOME ISSUES WITH THE BLUNT PLASTIC CANNULAS IN THAT WHEN THE NURSING STAFF ARE USING THEM TO DRAW UP MEDICATIONS FROM A VIAL THEY ARE PUSHING PART OF THE RUBBER STOPPER INTO THE BOTTLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14582240 ↗
  • MalfunctionMar 14, 2021Packaging Problem; Packaging Problem

    IT WAS REPORTED THAT AN UNSPECIFIED NUMBER OF SYRINGE 10ML LL W/BLUNT PLASTIC CAN HAD DAMAGED PACKAGING BEFORE USE. THE FOLLOWING WAS REPORTED BY THE INITIAL REPORTER: "THE CUSTOMER REPORTED ABOUT SEVERAL DAMAGED PACKAGES. THE CUSTOMER HAS EXPERIENCED THE SAME ISSUE BEFORE AND IS STRONGLY COMPLAINING THAT THE ISSUE HAS NOT BEEN RESOLVED."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11478696 ↗
  • MalfunctionDec 15, 2017Dull, Blunt; Structural Problem

    IT WAS REPORTED THAT THE STOPPER OF THE 10 ML SYRINGE WITH BD BLUNT PLASTIC CANNULA APPEARS TO BE ¿BREAKING DOWN¿ WHEN USING A PARTICULAR CONTRAST. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7122833 ↗

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 · Terminated
    BD 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 · Terminated
    BD Vacutainer Blood Collection Assembly with BD Blunt Plastic Cannula; Catalog #303380.

Other Needle, hypodermic, single lumen devices

All Needle, hypodermic, single lumen devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.