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# BD Recall of Alaris Pump Due to Keypad
- URL: https://www.fdaweb.com/bd-recall-of-alaris-pump-due-to-keypad/
- Published: 2021-04-16T12:00:00.000Z
- Updated: 2026-09-14T16:55:17.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149130

Becton Dickinson has recalled (Class 1) its CareFusion 303 Alaris Pump Module because of the risk of the keypad lifting up due to fluid entry. The issue could lead to keys that become unresponsive or stuck, and this may lead to an infusion delay or interruption, a[ recall notice ](https://www.fda.gov/medical-devices/medical-device-recalls/carefusion-303-inc-recalls-bd-alaris-pump-module-model-8100-due-risk-stuck-or-unresponsive-keys?ref=fdaweb.com)says. “High-risk patient populations who are receiving life-sustaining infusions are at the greatest risk of harm,” it says.

  
The infusion pump and vital signs monitoring system comprises a computer unit, the Guardrails Suite MX, and up to four removable infusion or monitoring modules (channels), according to the company. It is used to deliver fluids including medications, blood, or blood products, into a patient’s body in a controlled manner.