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# Class 1 Recall of Alaris Infusion Pump Bezel Assembly
- URL: https://www.fdaweb.com/class-1-recall-of-alaris-infusion-pump-bezel-assembly/
- Published: 2021-08-24T12:00:00.000Z
- Updated: 2026-09-14T17:11:41.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149992

FDA has classified as Class 1 a Bio-Medical Equipment Service Co. recall of the Alaris Infusion Pump Module Model 8100 pump bezel assembly and Alaris infusion pumps repaired with the bezel assembly due to the potential for the bezel components to crack or separate. The separation of one or more bezel posts may result in the free flow of fluids to a patient or an interruption of fluids delivered to a patient, a [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/bio-medical-equipment-service-co-recalls-alaris-infusion-pump-module-8100-bezel-due-possible-cracked?ref=fdaweb.com) says. The Alaris pump is used to deliver fluids such as medications, nutrients, blood, and other therapies into a person’s body in controlled amounts.