McKesson 102-N18105SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30612479178497), received between Jan 9, 2020 and Jan 9, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Activation 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 9, 2020Use of Device Problem; Activation Problem; Use of Device Problem; Activation Problem

  THE USER FACILITY REPORTED THAT A STAFF MEMBER WAS ENGAGING THE SAFETY FEATURE AND INSTEAD OF COVERING THE NEEDLE, THE SAFETY COVER BENT THE NEEDLE AND STUCK THE EMPLOYEE. ADDITIONAL INFORMATION WAS RECEIVED (B)(6) 2019: THE MD WAS DOING AN ASPIRATION AND USED HIS THUMB TO ENGAGE THE SAFETY DEVICE. THE SYRINGE WAS IN HIS HAND. INSTEAD OF LOCKING THE NEEDLE, NEEDLE BENT AND PIERCED HIS INDEX FINGER. NEEDLE WAS NOT BENT PRIOR TO ACTIVATION. PROCEDURE WAS COMPLETED SUCCESSFULLY. THE WOUND WAS WASHED, AND PRESENTED TO THE EMPLOYEE HEALTH FOR MONITORING.

  Patient problems: Needle Stick/Puncture; No Known Impact Or Consequence To Patient

  MAUDE report 9568802 ↗