Drug Recalls

Cardinal Health Recalls Monoject Saline Flush Prefilled Syringes for Risk of Air Re-entering Syringe Leading to Air Embolism

Posted on by Editor

Date: 08/23/2021

Product type: Null

Recalled Product

  • Monoject Flush Prefilled Syringes (0.9% sodium chloride)
  • Product Codes, All Lots:
    • Product Code (SKU) – Product Description:
      • 8881570121 – 12mL Syringe, 10mL Saline Fill
      • 8881570123 – 12mL Syringe, 3mL Saline Fill
      • 8881570125 – 12mL Syringe, 5mL Saline Fill
  • Distribution Dates: July 1, 2019 to July 1, 2021
  • Devices Recalled in the United States: 267,217,860
  • Date Initiated by Firm: August 4, 2021

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/cardinal-health-recalls-monoject-saline-flush-prefilled-syringes-risk-air-re-entering-syringe