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McKesson 102-SN3C2558SRecalls & reported problems

Mckesson Medical-Surgical Inc. · SYRINGE/NDL, SAFETY 3CC 25GX5/ · Class 2

Adverse event reports
5
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 20612479179084), received between Jul 19, 2018 and Nov 17, 2023 — classified as 5 malfunctions.

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

Reports received per month

Nov 2023: 2 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Activation Problem3
  • Break1
  • Use of Device Problem1

Patient problems

  • Needle Stick/Puncture4
  • No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 17, 2023Activation Problem; Activation Problem

    THE USER FACILITY REPORTED THAT THE SAFETY ON THE NEEDLE GOES OFF TO THE SIDE INSTEAD OF STRAIGHT DOWN TO COVER THE NEEDLE. AN EMPLOYEE WAS STUCK WITH THE NEEDLE BECAUSE THE SAFETY IS NOT VERY GOOD. 30 OCT 2023: STAFF MEMBER WAS NOT ACTIVATING AGAINST A HARD SURFACE WITHOUT WALKING AROUND WITH NEEDLE. THIS OCCURRED AFTER A SUCCESSFUL PATIENT INJECTION OF HIGH DOSE FLU VACCINE. THE SAFETY WENT TO THE SIDE OF THE NEEDLE AND THE NEEDLE BROKE OFF. STUCK INSIDE THE EMPLOYEES' FINGER. NO TESTING WAS PERFORMED TO DETERMINE BBP EXPOSURE. NEEDLE STICKS DID NOT REQUIRE ADDITIONAL TREATMENT ASIDE FROM FIRST AID. STAFF MEMBER CONDITION WAS STABLE.

    Patient problems: Needle Stick/Puncture; No Clinical Signs, Symptoms or Conditions

    MAUDE report 18166443 ↗
  • MalfunctionNov 17, 2023Activation Problem; Activation Problem

    THE USER FACILITY REPORTED THAT THE SAFETY ON THE NEEDLE GOES OFF TO THE SIDE INSTEAD OF STRAIGHT DOWN TO COVER THE NEEDLE. AN EMPLOYEE WAS STUCK WITH THE NEEDLE BECAUSE THE SAFETY IS NOT VERY GOOD. (B)(6)2023: STAFF MEMBER WAS NOT ACTIVATING AGAINST A HARD SURFACE WITHOUT WALKING AROUND WITH NEEDLE. THIS OCCURRED AFTER A SUCCESSFUL PATIENT INJECTION OF HIGH DOSE FLU VACCINE. THE SAFETY WENT TO THE SIDE OF THE NEEDLE AND THE NEEDLE BROKE OFF. STUCK INSIDE THE EMPLOYEES' FINGER. NO TESTING WAS PERFORMED TO DETERMINE BBP EXPOSURE. NEEDLE STICKS DID NOT REQUIRE ADDITIONAL TREATMENT ASIDE FROM FIRST AID. STAFF MEMBER CONDITION WAS STABLE.

    Patient problems: Needle Stick/Puncture; No Clinical Signs, Symptoms or Conditions

    MAUDE report 18166442 ↗
  • MalfunctionMay 4, 2022Break; Break

    THE USER FACILITY REPORTED THAT THE NEEDLE BROKE INSIDE THE VIAL WHEN THE PHYSICIAN PREPARED THE VACCINE. ADDITIONAL INFORMATION RECEIVED 07 APR 2022: THE DOCTOR WAS MIXING MEDICATION "PROQUAD" ASPIRATING FROM GLASS VIAL PRIOR TO THE VACCINE DELIVERY, WHEN ACCESSING THE MEDICATION, THE NEEDLE BROKE OFF AND FELL INTO THE VIAL. THEY LOOKED AT THE NEEDLE AND DID NOT SEE ANY BEND IN THE NEEDLE AND THEN DISPOSED THE NEEDLE AND VACCINE. THEY MIXED A NEW VACCINE TO RESOLVE THE ISSUE FOR PATIENT INJECTION. PATIENT WAS NOT IMPACTED IN ANY WAY AND IS STABLE/HEALTHY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14280659 ↗
  • MalfunctionDec 23, 2021Activation Problem; Activation Problem

    THE USER FACILITY REPORTED THAT AN EMPLOYEE WAS GIVING A B-12 INJECTION TO A PATIENT, AND WHEN THE EMPLOYEE WENT TO PUT THE SAFETY OVER THE NEEDLE, THE ENTIRE NEEDLE CAME OFF AND STUCK HER. ADDITIONAL INFORMATION WAS RECEIVED ON 02DECEMBER2021: IT WAS REPORTED THAT THE NEEDLE CAME OFF OF THE SYRINGE AND STUCK IN HER FINGER WHILE SHE WAS TRYING TO ACTIVATE THE SAFETY.

    Patient problems: Needle Stick/Puncture

    MAUDE report 13082363 ↗
  • MalfunctionJul 19, 2018Use of Device Problem; Use of Device Problem

    THE USER FACILITY REPORTED THAT THE NEEDLE WAS EXPOSED WHEN CAPPING. THE NEEDLE TURNS TOWARDS THE RIGHT WHEN CAPPING. WHICH CAUSED THE DOCTOR TO INCUR A NEEDLE STICK.

    Patient problems: Needle Stick/Puncture

    MAUDE report 7702219 ↗

Other Syringe, Antistick devices

All Syringe, Antistick devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.