Medline SYR100302Recalls & reported problems
Medline Industries, Inc. · NEEDLE,30GX0.5"REG,BEVEL · Class 2
- Adverse event reports
- 14
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 30080196305630), received between Mar 22, 2023 and Sep 29, 2026 — classified as 14 malfunctions.
The most frequently reported specific device problem is “Obstruction of Flow” (4 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
- Obstruction of Flow4
- Break2
- Fluid/Blood Leak2
- Material Twisted/Bent2
- Appropriate Device Problem Term/Code Not Available1
- Connection Problem1
- Loose or Intermittent Connection1
- Material Protrusion/Extrusion1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
- Needle Stick/Puncture3
- Foreign Body In Patient2
- Insufficient Information1
Recent adverse event reports
The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Fluid/Blood Leak; Connection Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934907 ↗MalfunctionSep 29, 2026Obstruction of Flow
It was reported that "clogging needles/syringes it has been an ongoing issue with the BD Luer lock 3 ml and the 30 gauge hypodermic needles. It occurs daily, sometimes multiple times with the same syringe and we keep having to change the needles as the syringe keeps clogging."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931962 ↗MalfunctionSep 28, 2026Obstruction of Flow
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50921538 ↗MalfunctionSep 24, 2026Obstruction of Flow
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50884449 ↗MalfunctionSep 23, 2026Obstruction of Flow
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50873872 ↗MalfunctionSep 18, 2026Material Twisted/Bent
It was reported that "the needle bent, and poked her finger through the cap.".
Patient problems: Needle Stick/Puncture
MAUDE report 50816899 ↗MalfunctionSep 15, 2026Material Puncture/Hole; Material Twisted/Bent
Patient problems: Needle Stick/Puncture
MAUDE report 50781436 ↗MalfunctionSep 14, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50756906 ↗MalfunctionSep 14, 2026Material Protrusion/Extrusion
It was reported that when the provider went to use the needle, the needle was not protected in the cap. The needle was sticking out past the cap causing the provider to be stuck by it.
Patient problems: Needle Stick/Puncture
MAUDE report 50754683 ↗MalfunctionAug 28, 2025Loose or Intermittent Connection; Loose or Intermittent Connection
THE NEEDLE TUBE WAS FALLEN OFF FROM THE SYRINGE WHEN INJECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22912003 ↗MalfunctionAug 22, 2025Break; Break
THE CUSTOMER REPORTED THAT THE NEEDLE BROKE INSIDE THE PATIENT'S BODY DURING INJECTION.
Patient problems: Foreign Body In Patient
MAUDE report 22871940 ↗MalfunctionJan 17, 2025Partial Blockage; Partial Blockage
CLOGGING NEEDLES/SYRINGES IT HAS BEEN AN ONGOING ISSUE WITH THE BD LUER LOCK 3 ML AND THE 30 GAUGE HYPODERMIC NEEDLES. IT OCCURS DAILY, SOMETIMES MULTIPLE TIMES WITH THE SAME SYRINGE AND WE KEEP HAVING TO CHANGE THE NEEDLES AS THE SYRINGE KEEPS CLOGGING. IT'S HAPPENING WITH ALL OF OUR PROVIDERS. UNFORTUNATELY, I NEED TO USE 3 ML SYRINGES AS I DO LARGER PROCEDURES, SO DON'T HAVE ANY OTHER ALTERNATIVE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21176018 ↗MalfunctionFeb 8, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
THE NEEDLE IS COMING OFF THE SYRINGE WHEN INJECTING LIDOCAINE TO THE PATIENT.
Patient problems: Insufficient Information
MAUDE report 18672764 ↗MalfunctionMar 22, 2023Break; Break
Other Needle, Hypodermic, Single Lumen devices
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- 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.