McKesson 102-N21105S3Recalls & reported problems
Mckesson Medical-Surgical Inc. · Safety Hypodermic Needles 21G x 1 1/2 in (100/bx, 8/cs) · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10612479246321), received between Apr 14, 2026 and Apr 14, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 14, 2026Detachment of Device or Device Component
TERUMO RECEIVED THE FOLLOWING REPORTED INFORMATION: THE SAFETY TOPS COME OFF, AND LEAKING FLUID AS IT IS BEING DRAWN INTO THE SYRINGE. THERE IS A POSSIBLE NEEDLE STICK ISSUE FROM THE SAFETY(S) COMING OFF. ADDITIONAL INFORMATION WAS RECEIVED ON 23-MAR-2026: THE SAFETY SHEATH IS REMOVAL OCCURS FOLLOWING ASPIRATION OR INJECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24873080 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.