SafetyGlide Syringe 303327Recalls & reported problems
Becton, Dickinson And Company · SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 00382903033270), received between Sep 4, 2025 and Jan 9, 2026 — classified as 13 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (10 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. 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
- Leak/Splash10
- Activation Problem1
- Contamination1
- Material Perforation1
Patient problems
- No Clinical Signs, Symptoms or Conditions12
- Needle Stick/Puncture1
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 9, 2026Material Perforation
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB NEEDLE WENT THROUGH THE SHILED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: RCC RECEIVED A COMPLAINT VIA EMAIL. FACILITY CONTACT: XXXXXX DEPARTMENT: MATERIALS MANAGEMENT XXXXXX. PRODUCT CATALOG NUMBER: 303327 PRODUCT DESCRIPTION: NEEDLE SYRINGE 0.375IN 1ML BD GENERAL-PURPOSE STERILE DISPOSABLE SAFETYGLIDE /NDL 27X3/8 IB. ORIGIN OF THE ISSUE: NURSING DETAIL: LOT #: EMPLOYEE HEALTH ALERTED SUPPLY CHAIN THAT EMPLOYEE "REPORTED HAVING SEVERAL NEAR MISSES WITH THIS ITEM BECAUSE THE SAFETY DIDN'T ENGAGE PROPERLY AND PUSHED THE NEEDLE AWAY INSTEAD OF COVERING IT" NUMBER OF OCCURRENCES: 2.0 SAMPLE AVAILABLE: NO. LOT NUMBER: 5160270L1. ADDITIONAL INFORMATION PROVIDED: ANY ADVERSE EVENT OR SERIOUS INJURY REPORTED TO PATIENT OR HEALTHCARE PROFESSIONAL? IF YES, PLEASE PROVIDE THE DETAILS. EMPLOYEE STUCK HERSELF WITH THE NEEDLE WHILE TRYING TO RECAP. SHE REPORTED PAST NEAR-MISSES FROM THE SAME SYSTEM PREVIOUSLY WHERE THE CAP DID NOT COVER THE TIP OF THE NEEDLE, BUT WE DON'T HAVE PREVIOUS REPORTS WITH LOT NUMBER INCRIMINATED. CAN YOU PLEASE PROVIDE AN EXACT DATE OF EVENT IN FORMAT DD-MMM-YYYY? 14/12/2025 PLEA
Patient problems: Needle Stick/Puncture
MAUDE report 24029902 ↗MalfunctionJan 7, 2026Activation Problem
MalfunctionNov 11, 2025Contamination; Contamination
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD FOREIGN MATTER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327 BATCH # UNKNOWN VERBATIM: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. PIECE OF PLASTIC TYPE MATERIAL IN SYRINGE. DISCOVERED WHEN DRAWING UP MEDICATION. NO HARM, DID NOT LEAVE PHARMACY, IDENTIFIED BY PHARMACY TECHNICIAN PRODUCT DESCRIPTION BD SAFETYGLIDE 1ML SYRINGE 27G 3/8' GREY CAP REF#303327.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23526202 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327, BATCH # 100484F1. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE, VNDR ITEM#: 303327, LOT#: 100484F1, QUANTITY: 1, UOM: 100/BX, CMT: LEAKING, ADTL.CMTS: EXP - 04/30/28.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22967612 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327 BATCH # 2355084G1. RCC RECEIVED A COMPLAINT VIA EMAIL. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE VNDR ITEM#: 303327 LOT#: 2355084G1 QUANTITY: 1 UOM: 100/BX CMT: LEAKING ADTL.CMTS: EXP - 11/30/27.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22967568 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327. BATCH # 3100484K1. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE. VNDR ITEM#: 303327. LOT#: 3100484K1. QUANTITY: (B)(4). UOM: (B)(4)/BX. CMT: LEAKING. ADTL.CMTS: EXP - 04/30/2028.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22965819 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327. BATCH # 2355084J1. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE. VNDR ITEM#: 303327. LOT#: 2355084J1. QUANTITY: (B)(4). UOM: (B)(4)/BX. CMT: LEAKING. ADTL.CMTS: EXP - 11/30/2027.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22965805 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327. BATCH # 3100484H1. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE VNDR ITEM#: 303327. LOT#: 3100484H1. QUANTITY: 1. UOM: 100/BX. CMT: LEAKING. ADTL.CMTS: EXP - 04/30/28.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22963469 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327. BATCH # 3100484J1. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE. VNDR ITEM#: 30332, LOT#: 3100484J1, QUANTITY: 1, UOM: 100/BX, CMT: LEAKING, ADTL.CMTS: EXP - 04/30/28.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22962229 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL# 303327, BATCH#: 2355084K1. RCC RECEIVED A COMPLAINT VIA EMAIL. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE, VNDR ITEM#: 303327, LOT#: 2355084K1, QUANTITY: 1, UOM: 100/BX, CMT: LEAKING, ADTL. CMTS: EXP: 11/30/2027.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22962202 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327. BATCH # 2355084H1. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE VNDR ITEM#: 303327. LOT#: 2355084H1. QUANTITY: (B)(4). UOM: (B)(4)/BX. CMT: LEAKING. ADTL.CMTS: EXP - 04/30/2028.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22962198 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327 BATCH # 2355084F1. RCC RECEIVED A COMPLAINT VIA EMAIL. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE VNDR ITEM#: 303327 LOT#: 2355084F1 QUANTITY: 1 UOM: 100/BX CMT: LEAKING ADTL.CMTS: EXP - 04/30/28.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22962186 ↗MalfunctionSep 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT THE BD SYRINGE SAFETYGLIDE 1ML W/NDL 27X3/8 IB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 303327 BATCH # 3100484G1. RCC RECEIVED A COMPLAINT VIA EMAIL. ITEM DESCRIPTION: SAFETYGLIDE TB SYR-NEEDLE VNDR ITEM#: 303327 LOT#: 3100484G1 QUANTITY: 1 UOM: 100/BX CMT: LEAKING ADTL.CMTS: EXP - 04/30/28.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22962184 ↗
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
Other Needle, hypodermic, single lumen devices
- BD Nano 2nd Gen 320550Becton Dickinson Pen Limited · Needle, hypodermic, single lumen2,044 reports
- BD SafetyGlide 305916Becton, Dickinson And Company · Needle, hypodermic, single lumen1,767 reports
- BD Nano Ultra-Fine 320122Becton Dickinson Pen Limited · Needle, hypodermic, single lumen601 reports
- N/A 305106Becton, Dickinson And Company · Needle, hypodermic, single lumen1 recall467 reports
- N/A 305110Becton, Dickinson And Company · Needle, hypodermic, single lumen418 reports
- BD Safe-Clip 328235Becton, Dickinson and Company Inc · Needle, hypodermic, single lumen268 reports
- BD Ultra-Fine 320109Becton Dickinson Pen Limited · Needle, hypodermic, single lumen229 reports
- BD AutoShield Duo 329515Becton, Dickinson And Company · Needle, hypodermic, single lumen208 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.
How reports and recalls are matched · Editorial policy · Report an error on this page