Pump Modules

  • May have been serviced with previously recalled bezel kit assemblies
  • Company: Becton, Dickinson and Company
  • Medical Devices
  • FDA
  • July 15, 2025

Product details

  • Pump Modules

Company announcement

BD (Becton, Dickinson and Company) issued a voluntary recall related to certain Alaris™ and BD Alaris™ Pump Modules.

The pump modules may have been serviced with previously recalled bezel kit assemblies.

This recall has been associated with incidents of serious injury and patient death.

Customers should immediately dispose of any affected bezel kit assemblies.

Risk:

These affected bezel kit assemblies were manufactured with a specific type of plastic material that weakens over time, leading to the potential of separated and/or broken bezel bosses that can cause free flow, over infusion, under infusion or interruption of infusion.

Impacted states: Nationwide

Products:

- Alaris™ and BD Alaris™ Pump Modules

Contact

For more information, call 1-844-823-5433.

View the original FDA notice

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