BD SafetyGlide 305951Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00382903059515), received between May 11, 2018 and Feb 11, 2021 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Device Markings/Labelling 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 11, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT SYRINGE ALRG SFTYGLD 1ML W/NDL 26X3/8 IB CAME WITH A MIX OF PRODUCT TYPES IN A PACK. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 305951 BATCH NO: 0141098. IT WAS REPORTED WE ARE STILL FINDING THE INSULIN SYRINGES IN STERILE BOXES DAILY. VERBATIM: WE OPENED THE BOXES ON 1/15/2021. WE ARE STILL FINDING THE INSULIN SYRINGES IN STERILE BOXES DAILY. NO ONE WAS INJURED. I HAD TO THROW AWAY SOME OF THE NEEDLES AS WE HAD CONTAMINATED THE NEEDLES WITH SERUM.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 11317334 ↗
• MalfunctionFeb 11, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT SYRINGE ALRG SFTYGLD 1ML W/NDL 26X3/8 IB CAME WITH A MIX OF PRODUCT TYPES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 305951 BATCH NO: 0141098. IT WAS REPORTED MIXED SYRINGES. VERBATIM: PER CUSTOMER'S RESPONSE ON 01/20/2021. WE OPENED THE BOXES ON 1/15/21. WE ARE STILL FINDING THE INSULIN SYRINGES IN STERILE BOXES DAILY. NO ONE WAS INJURED. I HAD TO THROW AWAY SOME OF THE NEEDLES AS WE HAD CONTAMINATED THE NEEDLES WITH SERUM. I WILL SEND THE NEEDLES THAT DID NOT GET CONTAMINATED VIA FEDEX. REPORTED ISSUE: REPORT THAT 1 CASE OF ITEM HAD MIXED SYRINGES IN EACH BOX. ABOUT 40 INSULIN SYRINGES WERE MIXED INTO THE CASE AND SHE CANNOT USE THESE. CUSTOMER DISPOSITION REQUEST: REPLACEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

  MAUDE report 11313534 ↗
• MalfunctionFeb 25, 2019Fail-Safe Problem

  IT WAS REPORTED THAT A 1 ML ALLERGIST TRAY WITH 26 G X 3/8 IN SAFETYGLIDE HAD A SAFETY MECHANISM THAT WOULD NOT ADVANCE ONTO THE NEEDLE AFTER USE. THIS OCCURRED ON 4 SEPARATE OCCASIONS BUT THE DATE/TIME AND OR PATIENT INFORMATION IS UNKNOWN.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8367249 ↗
• MalfunctionMay 11, 2018Difficult or Delayed Activation

  IT WAS REPORTED BY THE (B)(6) DEPARTMENT THAT THE BD SAFETYGLIDE¿ SYRING ALLERGIST TRAY PERMANENTLY ATTACHED NEEDLE ARE DIFFICULT TO ACTIVATE THE SAFETY MECHANISM FEATURE AFTER USE. NO REPORTS OF SERIOUS INJURY OR MEDICAL INTERVENTION NOTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7509338 ↗