McKesson 16-N22105Recalls & reported problems
Mckesson Medical-Surgical Inc. · Needle, Hypodermic TW, 22GX1 1/2 · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10612479206677), received between May 20, 2024 and May 9, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Complete Blockage” (3 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 Blockage3
- Blocked Connection1
- Dull, Blunt1
- Obstruction of Flow1
- Partial Blockage1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 9, 2026Obstruction of Flow
SEEM TO NOT BE RELEASING THE CONTENTS COMPLETELY, CAUSING THE PATIENTS TO HAVE TO BE PRICKED MULTIPLE TIMES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25132020 ↗MalfunctionOct 17, 2025Partial Blockage; Partial Blockage
THE CUSTOMER REPORTED THAT THE NEEDLES BECOME PLUGGED MID-PROCEDURE. THEY ATTEMPTED TO SIFT THROUGH VARIOUS NEEDLES TO IDENTIFY THE ISSUE. 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 23320965 ↗MalfunctionApr 29, 2025Complete Blockage; Complete Blockage
THE CUSTOMER REPORTED THAT THE FLUID COULD NOT PASS THROUGH THE NEEDLE DUE TO THE ABSENCE OF AN OPEN BEVEL AT THE BOTTOM WHERE THE FLUID EXITS. NO PATIENT INJURIES WERE SUSTAINED AS A RESULT OF THIS ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21925692 ↗MalfunctionApr 9, 2025Complete Blockage; Blocked Connection; Complete Blockage; Blocked Connection
IT WAS REPORTED BY THE CUSTOMER THAT THE SOLUTION WOULDN'T COME OUT OF NEEDLE WHEN PUSHED. AFTER REPLACING THE SYRINGE WITH NO IMPROVEMENT, IT WAS DETERMINED THAT THE PROBLEM ORIGINATED WITH THE NEEDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21803356 ↗MalfunctionMar 21, 2025Complete Blockage; Complete Blockage
IT WAS REPORTED BY THE CUSTOMER THAT THE SOLUTION WOULDN'T FLOW THROUGH THE NEEDLE WHEN PRESSURE WAS APPLIED. AFTER REPLACING THE SYRINGE WITHOUT IMPROVEMENT, IT WAS DETERMINED THAT THE ISSUE ORIGINATED WITH THE NEEDLE, WHICH THE CUSTOMER DESCRIBED AS BEING FULLY CLOGGED. NO INFORMATION HAS BEEN RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21661711 ↗MalfunctionMay 20, 2024Dull, Blunt; Dull, Blunt
THE CUSTOMER CLAIMS THAT SOME OF THE NEEDLES SEEM TO BE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19349112 ↗
Other Needle, Hypodermic, Single Lumen devices
- BD Nano 2nd Gen 320550Becton Dickinson Pen Limited · Needle, hypodermic, single lumen2,044 reports
- BD SafetyGlide 305916Becton, Dickinson And Company · Needle, hypodermic, single lumen1,767 reports
- BD Nano Ultra-Fine 320122Becton Dickinson Pen Limited · Needle, hypodermic, single lumen601 reports
- N/A 305106Becton, Dickinson And Company · Needle, hypodermic, single lumen1 recall467 reports
- N/A 305110Becton, Dickinson And Company · Needle, hypodermic, single lumen418 reports
- BD Safe-Clip 328235Becton, Dickinson and Company Inc · Needle, hypodermic, single lumen268 reports
- BD Ultra-Fine 320109Becton Dickinson Pen Limited · Needle, hypodermic, single lumen229 reports
- BD AutoShield Duo 329515Becton, Dickinson And Company · Needle, hypodermic, single lumen208 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page