McKesson 16-N2605Recalls & reported problems
Mckesson Medical-Surgical Inc. · Needle, Hypodermic TW, 26GX 1/2 · 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 10612479206820), received between Nov 20, 2024 and Nov 22, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Complete Blockage” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Complete Blockage1
- Partial Blockage1
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.
MalfunctionNov 22, 2024Complete Blockage; Complete Blockage
THE CUSTOMER REPORTED THAT NO FLUID IS RELEASED FROM THE NEEDLE DURING INJECTIONS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20756802 ↗MalfunctionNov 20, 2024Partial Blockage; Partial Blockage
IT WAS REPORTED BY THE CUSTOMER THAT NO FLUID IS RELEASED FROM THE NEEDLE DURING INJECTIONS. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20734854 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.