BD SafetyGlide 305907Recalls & reported problems
Becton, Dickinson And Company · SYRINGE 5ML LL W/NDL SFTYGLD 22X1-1/2 RB · 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 00382903059072), received between Jul 2, 2020 and Feb 3, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (2 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.
Most reported problems
Device problems
- Leak/Splash2
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
- No Patient Involvement1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 3, 2021Leak/Splash; Leak/Splash
IT WAS REPORTED THAT A SYRINGE 5ML LL W/NDL SFTYGLD 22X1-1/2 RB HAD A LOOSE STOPPER DURING USE. THE FOLLOWING WAS REPORTED BY THE INITIAL REPORTER: "SUSPECTED NEEDLE CORE RUBBER PLUG SLIPPING".
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient
MAUDE report 11276018 ↗MalfunctionJul 2, 2020Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE SYRINGE 5ML LL W/NDL SFTYGLD 22X1-1/2 RB EXPERIENCED A MISALIGNED/JAMMED/INSECURE STOPPER AND STOPPER DAMAGE/DEFORMATION. PRODUCT DEFECTS WERE NOTED PRIOR TO USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONGESTION DEFORMATION
Patient problems: No Patient Involvement
MAUDE report 10222540 ↗
Other SYRINGE, ANTISTICK devices
- BD Integra 305270Becton, Dickinson And Company · SYRINGE, ANTISTICK261 reports
- BD Integra 305271Becton, Dickinson And Company · SYRINGE, ANTISTICK106 reports
- BD Integra 305269Becton, Dickinson And Company · SYRINGE, ANTISTICK85 reports
- BD Luer-Lok, BD SafetyGlide 305924Becton, Dickinson And Company · SYRINGE, ANTISTICK1 recall28 reports
- BD Integra 305272Becton, Dickinson And Company · SYRINGE, ANTISTICK71 reports
- BD SafetyGlide 305945Becton, Dickinson And Company · SYRINGE, ANTISTICK63 reports
- BD SafetyGlide 305950Becton, Dickinson And Company · SYRINGE, ANTISTICK61 reports
- Medline SYRS101235FMedline Industries, Inc. · SYRINGE, ANTISTICK1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.