McKesson 102-N18105S3Recalls & reported problems
Mckesson Medical-Surgical Inc. · Safety Hypodermic Needles 18G x 1 1/2 in (100/bx, 8/cs) · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 10612479246291), received between Apr 3, 2025 and Apr 3, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Activation Problem” (2 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. 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
- Activation Problem2
Patient problems
- Needle Stick/Puncture1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 3, 2025Activation Problem; Activation Problem
THE USER FACILITY REPORTED THAT THE SAFETY HINGE WAS NOT FUNCTIONING PROPERLY, NO ONE WAS STUCK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21768686 ↗MalfunctionApr 3, 2025Activation Problem; Activation Problem
THE USER FACILITY REPORTED THAT THE SAFETY HINGE WAS NOT FUNCTIONING PROPERLY, RESULTING IN A NEEDLE STICK INCIDENT.
Patient problems: Needle Stick/Puncture
MAUDE report 21768671 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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