MEDLINE SSN100276Recalls & reported problems
Medline Industries, Inc. · NEEDLE,HYPODERM,SAFETY, 27GX1.25 · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10193489032024), received between Apr 13, 2023 and Sep 24, 2026 — classified as 2 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Infusion or Flow Problem” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available2
- Infusion or Flow Problem1
- Obstruction of Flow1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Insufficient Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Obstruction of Flow
It was reported that Dr has been using Medline brand 27G 1.25in needles (below) and he says that on multiple occasions he is unable to push steroids into the patient, while the needle is in the patient. The fluid will start to go in, then it will stop in the middle of the injection and just bounce back, like he is pushing against air.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50883909 ↗MalfunctionSep 21, 2026Infusion or Flow Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50841088 ↗InjuryFeb 13, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY THE NEEDLES HAVE CLOGGED ISSUES. THE MA DRAWS UP MEDICATION WITH A NEEDLE AND ATTACHES IT TO THE SYRINGE.
Patient problems: Insufficient Information
MAUDE report 21376349 ↗InjuryApr 13, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PER THE FACILITY "THE 27G NEEDLES ARE NOT DISPENSING ALL MEDICATION BEFORE IT STOPS WORKING, SO THE DOCTORS ARE HAVING TO INJECT THE PATIENT MORE THAN ONCE TO GIVE THE FULL DOSE".
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 16732072 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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