McKesson 102-N21105SRecalls & reported problems
Mckesson Medical-Surgical Inc. · NEEDLE, SAFETY 21GX1.5" (100/Bx) · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30612479178671), received between Jul 14, 2021 and Jul 14, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Activation Failure” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Activation Failure1
- Improper or Incorrect Procedure or Method1
- Positioning Failure1
Patient problems
- Needle Stick/Puncture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 14, 2021Positioning Failure; Improper or Incorrect Procedure or Method; Activation Failure; Positioning Failure; Improper or Incorrect Procedure or Method; Activation Failure
TERUMO MEDICAL RECEIVED AN FDA MEDWATCH REPORT MW# (B)(4). THE EVENT DESCRIPTION STATES: THE HYPODERMIC NEEDLE WAS USED BY A DOCTOR WHO CLOSED THE SAFETY SHIELD. THE NEEDLE WAS HANDED TO THE OR TECH AND THE SAFETY SHIELD WAS DEFECTIVE, CAUSING THE OR TECH TO BE STUCK BY THE NEEDLE. NEEDLE APPEARED CLOSED BUT HOUSING FLIPPED BACK. ADDITIONAL INFORMATION WAS RECEIVED ON 17JUNE2021: THE PATIENT WAS STABLE WITH NO RESIDUAL ISSUES. THE PATIENT RECEIVED ON SOURCE PATENT TESTING DUE TO THE NEEDLE STICK. THE NEEDLE WAS NOT ACTIVATED ON A HARD SURFACE. THE NEEDLE STICK CAUSED MINOR BLOOD LOSS. THE NEEDLE STICK WAS CLEANSED, OCCUPATIONAL HEALTH NOTIFIED, SOURCE PATIENT LAB RESULTS EVALUATED.
Patient problems: Needle Stick/Puncture
MAUDE report 12167035 ↗
Other Syringe, Antistick devices
- BD Integra 305270Becton, Dickinson And Company · SYRINGE, ANTISTICK261 reports
- BD Integra 305271Becton, Dickinson And Company · SYRINGE, ANTISTICK106 reports
- BD Integra 305269Becton, Dickinson And Company · SYRINGE, ANTISTICK85 reports
- BD Luer-Lok, BD SafetyGlide 305924Becton, Dickinson And Company · SYRINGE, ANTISTICK1 recall28 reports
- BD Integra 305272Becton, Dickinson And Company · SYRINGE, ANTISTICK71 reports
- BD SafetyGlide 305945Becton, Dickinson And Company · SYRINGE, ANTISTICK63 reports
- BD SafetyGlide 305950Becton, Dickinson And Company · SYRINGE, ANTISTICK61 reports
- Medline SYRS101235FMedline Industries, Inc. · SYRINGE, ANTISTICK1 recall0 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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