Medline PAIN8017Recalls & reported problems
Medline Industries, Inc. · NEEDLE, QUINCKE, 22GX3.5" · Class 2
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10884389622261), received between Apr 14, 2026 and Sep 29, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (3 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
- Material Twisted/Bent3
- Difficult to Open or Remove Packaging Material2
- Obstruction of Flow2
- Appropriate Device Problem Term/Code Not Available1
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936101 ↗MalfunctionSep 23, 2026Appropriate Device Problem Term/Code Not Available
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50875475 ↗MalfunctionSep 23, 2026Obstruction of Flow
It was reported that the needle clogs and will not push the medication.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870576 ↗MalfunctionSep 23, 2026Obstruction of Flow
It was reported that the needle clogs and will not push the medication.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870237 ↗MalfunctionSep 16, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50795391 ↗MalfunctionSep 14, 2026Break; Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765362 ↗MalfunctionApr 14, 2026Difficult to Open or Remove Packaging Material
THE PACKAGE TEARS ABOUT HALFWAY MAKING IT HARD TO SLIDE THE NEEDLE OUT OR IT CONTAMINATES BY FLIPPING OUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24880306 ↗MalfunctionApr 14, 2026Difficult to Open or Remove Packaging Material
THE PACKAGE TEARS ABOUT HALFWAY MAKING IT HARD TO SLIDE THE NEEDLE OUT OR IT CONTAMINATES BY FLIPPING OUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24880208 ↗
Other NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) devices
- ARROW IPN922632Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)2 recalls0 reports
- ARROW IPN922603Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- ARROW IPN922605Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- 22G 1 1/2IN Regional Block Needle 408348Becton, Dickinson And Company · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- ARROW IPN923597Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- ARROW IPN922631Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- ARROW IPN922604Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- BD QUINCKE Spinal Needles 405180Becton, Dickinson And Company · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)23 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.