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BD Luer-Lok, BD Eclipse 305778Recalls & reported problems

Becton, Dickinson And Company · SYRINGE 1ML LL W/NDL ECLIPSE 30x1/2 RB · Class 2

Adverse event reports
5
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00382903057788), received between Feb 7, 2019 and Apr 24, 2024 — classified as 3 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Retraction Problem” (3 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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 3 reportsMar 2024: 0 reportsApr 2024: 1 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: 0 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 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Retraction Problem3
  • Fluid/Blood Leak1
  • Loose or Intermittent Connection1
  • Material Protrusion/Extrusion1

Patient problems

  • Needle Stick/Puncture4
  • 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.

  • InjuryApr 24, 2024Material Protrusion/Extrusion; Material Protrusion/Extrusion

    IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 30X1/2 RB SAFETY MECHANISM FAILED IT WAS REPORTED BY THE CUSTOMER THAT POST SAFETY ENGAGEMENT. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. PLEASE SEE ATTACHMENT WITH SBAR AND PHOTOS.

    Patient problems: Needle Stick/Puncture

    MAUDE report 19173963 ↗
  • InjuryFeb 1, 2024Retraction Problem; Retraction Problem

    IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 30X1/2 RB HAD A SAFETY MECHANISM FAILURE. IT WAS REPORTED BY THE CUSTOMER REPORT NEEDLE STICK INJURY. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. PRODUCT CONCERN TICKET NUMBER: (B)(4). DATE OF INCIDENT: (B)(6) 2023. HOSPITAL: (B)(6) HOSPITAL. DEPARTMENT: 2 NORTH ACIU. PRODUCT: SAFETY SYRINGE 1CC. VMID: 305778. PRODUCT EXPIRY DATE: N/A. NUMBER OF DEFECTIVE PRODUCT(S): 1. IS SAMPLE AVAILABLE: YES. CONCERN DESCRIPTION: THE LOCK MECHANISM ON THE SYRINGE FAILED AND WE HAD 3 STAFF REPORT NEEDLE STICK INJURY.

    Patient problems: Needle Stick/Puncture

    MAUDE report 18628500 ↗
  • InjuryFeb 1, 2024Retraction Problem; Retraction Problem

    IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 30X1/2 RB HAD A SAFETY MECHANISM FAILURE IT WAS REPORTED BY THE CUSTOMER REPORT NEEDLE STICK INJURY. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. PRODUCT CONCERN TICKET NUMBER: (B)(4). DATE OF INCIDENT: (B)(6) 2023 HOSPITAL: (B)(6). DEPARTMENT: (B)(6). PRODUCT: SAFETY SYRINGE 1CC VMID: 305778 LOT NUMBER: PRODUCT EXPIRY DATE: N/A NUMBER OF DEFECTIVE PRODUCT(S): 1 IS SAMPLE AVAILABLE: YES CONCERN DESCRIPTION: THE LOCK MECHANISM ON THE SYRINGE FAILED AND WE HAD 3 STAFF REPORT NEEDLE STICK INJURY.

    Patient problems: Needle Stick/Puncture

    MAUDE report 18628460 ↗
  • MalfunctionFeb 1, 2024Retraction Problem; Retraction Problem

    IT WAS REPORTED THAT BD SYRINGE 1ML LL W/NDL ECLIPSE 30X1/2 RB HAD A SAFETY MECHANISM FAILURE IT WAS REPORTED BY THE CUSTOMER REPORT NEEDLE STICK INJURY. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. PRODUCT CONCERN TICKET NUMBER: (B)(4). DATE OF INCIDENT: (B)(6) 2023 HOSPITAL: (B)(6) DEPARTMENT: (B)(6) PRODUCT: SAFETY SYRINGE 1CC VMID: 305778 LOT NUMBER: PRODUCT EXPIRY DATE: N/A NUMBER OF DEFECTIVE PRODUCT(S): 1 IS SAMPLE AVAILABLE: YES CONCERN DESCRIPTION: THE LOCK MECHANISM ON THE SYRINGE FAILED AND WE HAD 3 STAFF REPORT NEEDLE STICK INJURY.

    Patient problems: Needle Stick/Puncture

    MAUDE report 18628458 ↗
  • MalfunctionFeb 7, 2019Fluid/Blood Leak; Loose or Intermittent Connection

    IT WAS REPORTED THAT A 30 G X 1/2 IN. BD ECLIPSE¿ 1 ML BD LUER-LOK¿ SYRINGE WITH DETACHABLE NEEDLE HAD A LOOSE PLUNGER AND DISCHARGED MEDICATION FROM THE PLUNGER.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8317247 ↗

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.