BD SafetyGlide 305908Recalls & reported problems
Becton, Dickinson And Company · SYR 10ML LL W/NDL SFTYGLD 22X1-1/2 RB · Class 2
All models of BD SafetyGlide (17)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382903059089), received between Aug 25, 2020 and Sep 26, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break1
- Defective Component1
- Leak/Splash1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient1
- No Patient Involvement1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 26, 2023Defective Component; Material Deformation; Defective Component; Material Deformation
IT WAS REPORTED THAT THE STOPPER IN THE BD LUER-LOK¿ SYRINGE WITH BD SAFETYGLIDE¿ NEEDLE WAS DEFORMED/TWISTED, CAUSING AN INACCURATE VOLUME OF MEDICATION TO BE DISPENSED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "ON 01SEP2023, A DEFECTIVE SYRINGE WAS ENCOUNTERED WHILE PERFORMING A LABORATORY TEST. THE RUBBER STOPPER IN THE BARREL WAS MORPHED/TWISTED WHICH CAUSED AN INACCURATE VOLUME TO BE DISPENSED."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17821693 ↗MalfunctionFeb 3, 2021Leak/Splash; Leak/Splash
IT WAS REPORTED THAT A SYR 10ML 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 11276047 ↗MalfunctionAug 25, 2020Break; Break
IT WAS REPORTED THAT NEEDLE WAS DISCOVERED TO BE BROKEN PRIOR TO USE WITH A 1 ML BD SAFETYGLIDE¿ INSULIN SYRINGE WITH ATTACHED NEEDLE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: BROKEN NEEDLE.
Patient problems: No Patient Involvement
MAUDE report 10448161 ↗
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 SYRS103225Medline Industries, Inc. · SYRINGE, ANTISTICK1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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