McKesson 16-N2705Recalls & reported problems
Mckesson Medical-Surgical Inc. · Needle, Hypodermic TW, 27GX 1/2 · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10612479206851), received between Apr 14, 2024 and Sep 9, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information2
- Complete Blockage1
- Fluid/Blood Leak1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 9, 2026Fluid/Blood Leak
Customer reported having a lot of issues with the needles not working with the syringes. Per customer response: The needles when attached to these syringes(1 cc syringes) do not fit securely and we have had medication spilling out because of the pressure between the syringe and needle when administering, it pops out.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50687293 ↗MalfunctionAug 27, 2026Complete Blockage
Customer stated that the needles seem to be blocked.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50466115 ↗MalfunctionApr 14, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
THE CUSTOMER REPORTED THAT THE CLIENT REPORTED THAT AFTER THE INJECTION, WHEN THE NURSE PUT ON THE PROTECTIVE CAP AGAIN, THE NEEDLE PIERCED THE PROTECTIVE CAP AND HURT THE HAND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102950 ↗MalfunctionApr 14, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
THE CUSTOMER REPORTED THAT THE CLIENT REPORTED THAT AFTER THE INJECTION, WHEN THE NURSE PUT ON THE PROTECTIVE CAP AGAIN, THE NEEDLE PIERCED THE PROTECTIVE CAP AND HURT THE HAND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102888 ↗
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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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