SafetyGlide 303326Recalls & reported problems
Becton, Dickinson And Company · SYR 3ML LL W/NDL SFTYGLD 23X1-1/2 RB TW · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00382903033263), received between Jul 25, 2024 and Aug 13, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Difficult or Delayed Activation” (2 reports).
4 other recalls cover devices cleared under the same FDA submission (K951254); they may or may not involve this specific model.
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
- Difficult or Delayed Activation2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 13, 2024Difficult or Delayed Activation; Difficult or Delayed Activation
MATERIAL# 303326 BATCH# 4010391 IT WAS REPORTED BY CUSTOMER THAT THE NEEDLE ITSELF IS VERY FLIMSY AND BENDS EASILY. THE SAFETY DEVICE IS DIFFICULT TO ENGAGE BECAUSE THAT IS ALSO FLIMSY AND BENDS THE NEEDLE AS YOU ARE ENGAGING THE SAFETY DEVICE. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED IT IS THE BD SAFETYGLIDE 3ML SYRINGE. REF 303326. THE NEEDLE ITSELF IS VERY FLIMSY AND BENDS EASILY. THE SAFETY DEVICE IS DIFFICULT TO ENGAGE BECAUSE THAT IS ALSO FLIMSY AND BENDS THE NEEDLE AS YOU ARE ENGAGING THE SAFETY DEVICE. LOT NUMBER - 4010391 CUSTOMER RESPONSE ON AUGUST 05, 2024 THIS IS BEING SHIPPED TODAY. THEY ARE DIFFERENT LOT NUMBERS BUT STILL SAME ISSUE. CUSTOMER RESPONSE ON AUGUST 09, 2024 I DIDN'T WRITE DOWN THE LOT NUMBER THAT I PUT IN THE BOX. YOU'LL HAVE TO CHECK THAT UPON ARRIVAL. I CAN'T GUARANTEE THE ONE I WOULD GIVE YOU OFF THE SHELF IS THE SAME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19974621 ↗MalfunctionJul 25, 2024Difficult or Delayed Activation; Difficult or Delayed Activation
MATERIAL# 303326 . BATCH# 4010391. IT WAS REPORTED BY CUSTOMER THAT THE NEEDLE ITSELF IS VERY FLIMSY AND BENDS EASILY. THE SAFETY DEVICE IS DIFFICULT TO ENGAGE BECAUSE THAT IS ALSO FLIMSY AND BENDS THE NEEDLE AS YOU ARE ENGAGING THE SAFETY DEVICE. RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. IT IS THE BD SAFETYGLIDE 3ML SYRINGE. REF 303326. THE NEEDLE ITSELF IS VERY FLIMSY AND BENDS EASILY. THE SAFETY DEVICE IS DIFFICULT TO ENGAGE BECAUSE THAT IS ALSO FLIMSY AND BENDS THE NEEDLE AS YOU ARE ENGAGING THE SAFETY DEVICE. LOT NUMBER - 4010391.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19827847 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K951254. One submission often covers many models, so check the product and lot details in each record.
- Z-2889-2020 · Jul 28, 2020 · TerminatedBD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
- Z-0315-2018 · Jul 5, 2017 · TerminatedSafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in Centurion Convenience Kits. Centurion component code BD17O1NS.
- Z-3116-2017 · Jun 13, 2017 · TerminatedBD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be used for general purpose injection, aspiration of fluids from
- Z-2748-2017 · Sep 16, 2016 · TerminatedBD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle is intended to be used for general purpose injection, aspiration of fluids from parts of the body below th
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.