McKesson 16-N251Recalls & reported problems
Mckesson Medical-Surgical Inc. · Needle, Hypodermic TW, 25GX1 · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10612479206738), received between Dec 25, 2025 and Feb 5, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Complete Blockage” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Complete Blockage2
- Partial Blockage1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 5, 2026Complete Blockage
IT WAS REPORTED BY THE CUSTOMER THAT THEY CANNOT PUSH MEDICATION THROUGH THE NEEDLE. 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 24267949 ↗MalfunctionJan 4, 2026Complete Blockage
THE CUSTOMER REPORTED THAT THE NEEDLES INJECT APPROXIMATELY 0.5 TO 1 ML AND THEN STOP, REQUIRING MULTIPLE NEEDLE INSERTIONS TO COMPLETE THE INJECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23954145 ↗MalfunctionDec 25, 2025Partial Blockage; Partial Blockage
THE CUSTOMER REPORTED THAT THE NEEDLES INJECT APPROXIMATELY 0.5 TO 1 ML AND THEN STOP, REQUIRING MULTIPLE NEEDLE INSERTIONS TO COMPLETE THE INJECTION. 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 23892266 ↗
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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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