SafetyGlide Insulin Syringe 305934Recalls & reported problems
Becton, Dickinson And Company · SafetyGlide™ Insulin Syringes, U-100, 8mm, 30G, 0.5mL · Class 2
All models of SafetyGlide Insulin Syringe (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00382903059348), received between Oct 31, 2018 and Sep 28, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Packaging Problem” (4 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Packaging Problem4
- Contamination /Decontamination Problem2
- Break1
- Crack1
- Difficult or Delayed Activation1
- Low Sensing Threshold1
- Material Protrusion/Extrusion1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- No Known Impact Or Consequence To Patient3
- No Information1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Packaging Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50926301 ↗MalfunctionSep 28, 2026Packaging Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50926113 ↗MalfunctionSep 28, 2026Packaging Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50925412 ↗MalfunctionSep 28, 2026Packaging Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50923798 ↗MalfunctionJul 11, 2025Low Sensing Threshold; Material Protrusion/Extrusion; Low Sensing Threshold; Material Protrusion/Extrusion
AFTER INJECTION, THE LOCKING ARM CANNOT COVER THE NEEDLE AND THE NEEDLE IS CROOKED. NEEDLE STICK BY THE NURSE. SAMPLE AVAILABILITY: YES. SAMPLE AVAILABILITY DETAILS: PICTURE/VIDEO AVAILABLE AND PHYSICAL SAMPLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22482373 ↗MalfunctionDec 19, 2018Contamination /Decontamination Problem
IT WAS REPORTED THAT A 1/2 ML BD SAFETYGLIDE¿ INSULIN SYRINGE WITH 30G X 5/16 NEEDLE HAD A "BEAD" INSIDE THE SYRINGE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8181216 ↗MalfunctionDec 7, 2018Difficult or Delayed Activation; Difficult or Delayed Activation
IT WAS REPORTED THAT A 1/2 ML BD SAFETYGLIDE¿ INSULIN SYRINGE WITH 30G X 5/16 IN ATTACHED NEEDLE HAD A SAFETY SHIELD DEVICE LOCK.
Patient problems: No Information
MAUDE report 8143631 ↗MalfunctionNov 13, 2018Contamination /Decontamination Problem
IT WAS REPORTED THAT BD SAFETYGLIDE¿ INSULIN SYRINGE PACKAGE DIDN'T SEAL WELL, AND THE SYRINGE WAS CONTAMINATED. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8067863 ↗MalfunctionOct 31, 2018Break; Crack
IT WAS REPORTED THAT A BD SAFETYGLIDE¿ INSULIN SYRINGE HAD A CRACKED AND BROKEN BARREL. THERE WAS NO REPORT OF EXPOSURE, SERIOUS INJURY, OR MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8026185 ↗
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 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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