SafetyGlide Insulin Syringe 305935Recalls & reported problems
Becton, Dickinson And Company · SafetyGlide™ Insulin Syringes, U-100, 12.7mm, 29G, 0.3mL · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00382903059355), received between Apr 8, 2024 and Dec 4, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Activation Problem” (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.
Reports received per month
Most reported problems
Device problems
- Activation Problem2
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 4, 2025Activation Problem; Activation Problem
MalfunctionDec 4, 2025Activation Problem; Activation Problem
MalfunctionMay 6, 2024Material Separation; Material Separation
MATERIAL: 305935 BATCH#: 3216615 IT WAS REPORTED THAT THE SYRINGE 0.3ML 29GA 1/2IN BLS 400 SG STOPPER SEPARATED FROM THE PLUNGER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED BY THE CUSTOMER THAT WHEN THE INSULIN WAS DRAWN UP, IT WAS OBSERVED THAT THE PLUNGER WAS IN 2 PIECES, AS EVIDENCED BY SEPARATION IN THE FLUID. NOT USED ON PATIENT. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. PROCEDURE- ADMINISTRATION OF INSULIN. WHEN THE INSULIN WAS DRAWN UP, IT WAS OBSERVED THAT THE PLUNGER WAS IN 2 PIECES, AS EVIDENCED BY SEPARATION IN THE FLUID. NOT USED ON PATIENT. PRODUCT#: 305935 LOT: 3216615R1 ADDITIONAL INFORMATION PROVIDED ON 05/01/2024: "PLUNGER/ROD INTACT AND NOT DAMAGED. STOPPER WAS BROKEN IN 2 PIECES. 1 PIECE ATTACHED TO PLUNGER AND THE OTHER WAS FLOATING ON THE INSULIN THAT WAS IN THE SYRINGE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19249479 ↗MalfunctionApr 8, 2024
PROCEDURE- ADMINISTRATION OF INSULIN. WHEN THE INSULIN WAS DRAWN UP, IT WAS OBSERVED THAT THE PLUNGER WAS IN 2 PIECES, AS EVIDENCED BY SEPARATION IN THE FLUID. NOT USED ON PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19058691 ↗
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.