McKesson 192-N2558SRecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10612479248561), received between Sep 16, 2022 and Mar 20, 2023 — classified as 4 injuries, 1 malfunction.

The most frequently reported specific device problem is “Material Protrusion/Extrusion” (4 reports).

4 other recalls cover devices cleared under the same FDA submission (K951254); they may or may not involve this specific model.

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

• InjuryMar 20, 2023Material Protrusion/Extrusion; Material Protrusion/Extrusion

  IT WAS REPORTED WHILE USING BD SAFETYGLIDE¿ NEEDLE THE SAFETY MECHANISM WAS DIFFICULT TO ENGAGE. THIS IS 3 OF 4 RELATED INCIDENTS. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: OVER THE PAST FEW MONTHS, WE HAVE HAD SEVERAL NURSES TO EXPERIENCE SHARPS INJURIES WHILE USING THIS PRODUCT. THE SAFETY MECHANISM IS HARD TO ACTIVATE AND SOMETIMES ONCE IT IS ACTIVATED, IT DOES NOT STAY CLOSED OVER THE SHARP END OF THE NEEDLE. THESE INCIDENTS OCCURRED FROM 11.28.22 THROUGH 02.24.23. THERE WERE A TOTAL OF 4 INCIDENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16575596 ↗
• InjuryMar 20, 2023Material Protrusion/Extrusion; Material Protrusion/Extrusion

  IT WAS REPORTED WHILE USING BD SAFETYGLIDE¿ NEEDLE THE SAFETY MECHANISM WAS DIFFICULT TO ENGAGE WHICH RESULTED IN A NEEDLE STICK. THIS IS 2 OF 4 INCIDENTS. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: OVER THE PAST FEW MONTHS, WE HAVE HAD SEVERAL NURSES TO EXPERIENCE SHARPS INJURIES WHILE USING THIS PRODUCT. THE SAFETY MECHANISM IS HARD TO ACTIVATE AND SOMETIMES ONCE IT IS ACTIVATED, IT DOES NOT STAY CLOSED OVER THE SHARP END OF THE NEEDLE. THERE WERE A TOTAL OF 4 INCIDENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16575513 ↗
• InjuryMar 20, 2023Material Protrusion/Extrusion; Material Protrusion/Extrusion

  IT WAS REPORTED WHILE USING BD SAFETYGLIDE¿ NEEDLE THE SAFETY MECHANISM WAS DIFFICULT TO ENGAGE AND A NEEDLESTICK OCCURRED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: SAFETY MECHANISM IS HARD TO ACTIVATE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16574169 ↗
• InjuryMar 18, 2023Material Protrusion/Extrusion; Material Protrusion/Extrusion

  IT WAS REPORTED WHILE USING BD SAFETYGLIDE¿ NEEDLE THE SAFETY MECHANISM WAS DIFFICULT TO ENGAGE, WHICH RESULTED IN NEEDLE STICK INJURY. THIS IS 1 OF 4 RELATED COMPLAINTS. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: OVER THE PAST FEW MONTHS, WE HAVE HAD SEVERAL NURSES TO EXPERIENCE SHARPS INJURIES WHILE USING THIS PRODUCT. THE SAFETY MECHANISM IS HARD TO ACTIVATE AND SOMETIMES ONCE IT IS ACTIVATED, IT DOES NOT STAY CLOSED OVER THE SHARP END OF THE NEEDLE. THESE INCIDENTS OCCURRED FROM 11.28.22 THROUGH 02.24.23. THERE WERE A TOTAL OF 4 INCIDENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16569869 ↗
• MalfunctionSep 16, 2022Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT 3 BD SAFETYGLIDE¿ NEEDLES CLOGGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WHEN THEY ARE ADDING SAFETY NEEDLE TO PRE DRAWN SYRINGE THEY ARE UNABLE TO REMOVE THE AIR, NOTHING COMES OUT OF NEEDLE, THERE IS TOO MUCH PRESSURE.

  Patient problems: Insufficient Information

  MAUDE report 15442014 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K951254. One submission often covers many models, so check the product and lot details in each record.

• Z-2889-2020 · Jul 28, 2020 · Terminated
  BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
• Z-0315-2018 · Jul 5, 2017 · Terminated
  SafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in Centurion Convenience Kits. Centurion component code BD17O1NS.
• Z-3116-2017 · Jun 13, 2017 · Terminated
  BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be used for general purpose injection, aspiration of fluids from
• Z-2748-2017 · Sep 16, 2016 · Terminated
  BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle is intended to be used for general purpose injection, aspiration of fluids from parts of the body below th