McKesson 102-SN3C251SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20612479179114), received between Jun 7, 2018 and Jun 7, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Bent” (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.

• MalfunctionJun 7, 2018Bent; Break; Use of Device Problem; Bent; Break; Use of Device Problem

  THE USER FACILITY REPORTED THE SAFETY IS NOT ENGAGING WHEN CLICKED. THE NURSE ACTUALLY BROKE THE NEEDLE WHEN TRYING TO GET THE SAFETY TO ENGAGE. THE NEEDLE WAS FLIMSY AND THE SAFETY DOESN'T ALWAYS LATCH. ADDITIONAL INFORMATION RECEIVED ON 5/23/18: THE NEEDLE WAS BEING USED FOR A DEPO-PROVERA SHOT. AS THE NEEDLE WAS BEING REMOVED FROM THE PATIENT IT HAD BENT. THEN WHEN THE NURSE WENT TO ENGAGE THE SAFETY THE NEEDLE BROKE OFF. THERE WAS NO NEEDLE STICK, THE NEEDLE JUST APPEARED TO BE FLIMSY AND THE SAFETY DID NOT LATCH. THERE WAS NO IMPACT TO THE PATIENT OR PROCEDURE AS THE PATIENT RECEIVED THE INTENDED DOSE OF MEDICATION.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7577697 ↗