BD SafetyGlide 305909Recalls & reported problems
Becton, Dickinson And Company · SYR 3ML LL W/NDL SFTYGLD 21X1-1/2 RB TW · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00382903059096), received between Mar 12, 2018 and Apr 15, 2026 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Delivered as Unsterile Product” (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
- Delivered as Unsterile Product2
- Activation Problem1
- Crack1
Patient problems
- No Known Impact Or Consequence To Patient2
- Exposure to Body Fluids1
- Insufficient Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 15, 2026Activation Problem
MalfunctionMar 25, 2020Delivered as Unsterile Product; Delivered as Unsterile Product
IT WAS REPORTED THAT PRIOR TO USE MISSING SAFETY SHIELD WAS DISCOVERED AND STERILITY MAY BE COMPROMISED WITH A BD SAFETYGLIDE¿ SYRINGE W/NEEDLE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED THAT NEEDLE IS MISSING THE SAFETY SHIELD.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9880054 ↗MalfunctionMar 18, 2020Delivered as Unsterile Product; Delivered as Unsterile Product
IT WAS REPORTED THAT STERILE BREACH OCCURRED BEFORE USE WITH A BD INSYTE¿ CATHETER I.V. 24GA X 0.75¿ (0.7 X 19 MM). THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, "WHILE PUTTING THIS PRODUCT AWAY, WE NOTICED THE TIP OF A BENT NEEDLE STICKING THRU THE PACKAGE. ALL 3 ITEMS WERE IN THIS SAME SEALED PACKAGE. I TOOK THEM OUT OF THIS SEALED PACKAGE, TO SEND YOU PICTURES. SO FAR, THIS IS AN ISOLATED INCIDENT, BUT WANTED YOU TO BE AWARE, IN CASE THERE ARE OTHERS. PLEASE LET ME KNOW IF YOU NEED ADDITIONAL INFORMATION."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9850344 ↗InjuryMar 12, 2018Crack
IT WAS REPORTED THAT DURING ADMINISTRATION OF OMALIZUMAB USING A BD SYRINGE WITH SAFETYGLIDE¿ SHIELDING HYPODERMIC NEEDLE, THE SIDE BARREL OF THE SYRINGE CRACKED AND THE EMPLOYEE WAS SPLASHED IN THE EYE. EMPLOYEE SOUGHT ADVICE FROM OCCUPATIONAL HEALTH BUT THERE WAS NO REPORT OF MEDICAL INTERVENTIONS.
Patient problems: Exposure to Body Fluids
MAUDE report 7331285 ↗
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.