McKesson 16-SN3C231Recalls & reported problems
Mckesson Medical-Surgical Inc. · Syringe/NDL, LL, 3cc · Class 2
Data updated Oct 16, 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 10612479207186), received between Apr 13, 2024 and May 8, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Compatibility 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
- Compatibility Problem1
- 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.
MalfunctionMay 8, 2024Partial Blockage; Partial Blockage
IT WAS REPORTED BY THE CUSTOMER THAT THE SYRINGE PLUNGER WAS GETTING STUCK ? - ? WAY DOWN THE SYRINGE WHILE ADMINISTERING AN INJECTION AND THE INJECTION COULD NOT BE COMPLETED.THE INJECTION HAD TO BE DISCONTINUED.THE CUSTOMER INDICATED THAT THERE WAS NO ISSUE WITH DRAWING UP THE MEDICATION INTO THE SYRINGE AND THERE WAS NO CONCERN OF INACCURATE DOSAGE BEING INJECTED WHEN THIS ISSUE OCCURRED.NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19266441 ↗MalfunctionApr 13, 2024Compatibility Problem; Compatibility Problem
THE CLIENT REPORTS THAT THE SYRINGE PLUNGER IS STUCK 1/2-3/4 OF THE WAY DOWN THE SYRINGE WHEN INJECTING AND CANNOT CONTINUE TO COMPLETE THE INJECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102835 ↗
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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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