> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# Pacific Medical Recalls Alaris Pump Front Bezel
- URL: https://www.fdaweb.com/pacific-medical-recalls-alaris-pump-front-bezel/
- Published: 2021-04-30T12:00:00.000Z
- Updated: 2026-09-14T16:57:05.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149231

Pacific Medical Group has recalled the Alaris Infusion Pump Module Model 8100 Front Bezel because components may crack or separate, leading to inaccurate delivery of fluids to patients. The pump is used to deliver fluids such as medications, nutrients, blood, and other therapies into a patient’s body in controlled amounts. The front bezel component is critical to the device’s proper performance, according to a [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/pacific-medical-group-dba-avante-health-solutions-recalls-alaris-infusion-pump-module-8100-bezel-due?ref=fdaweb.com), noting that they have been used to service and repair infusion pump modules.