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# Class 1 Recall of Alaris Pump Bezels
- URL: https://www.fdaweb.com/class-1-recall-of-alaris-pump-bezels/
- Published: 2021-06-16T12:00:00.000Z
- Updated: 2026-09-14T17:03:43.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149547

FDA has classified as Class 1 a recall of the Alaris Infusion Pump Module Model 8100 Bezel, purchased or installed by Infusion Pump Repair. Infusion Pump Repair is recalling the affected products and devices because the bezel components may crack or separate, leading to inaccurate delivery of fluids to patients. The separation of one or more bezel posts could allow over- or under-delivery of fluids, or it could interrupt fluid delivery altogether, a [recall notice ](https://www.fda.gov/medical-devices/medical-device-recalls/infusion-pump-repair-recalls-alaris-infusion-pump-module-8100-bezel-due-possible-cracked-or?ref=fdaweb.com)says. The Alaris infusion pump is used to deliver medications, nutrients, blood, and other therapies into a person’s body in controlled amounts. The bezel component is critical to the proper performance of the infusion pump. Bezels from Infusion Pump Repair are used to service and repair infusion pump modules.