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# Tenacore Recalls Alaris Pumps Over Bezel Posts
- URL: https://www.fdaweb.com/tenacore-recalls-alaris-pumps-over-bezel-posts/
- Published: 2021-04-19T12:00:00.000Z
- Updated: 2026-09-14T16:55:23.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149135

Tenacore is recalling Alaris Pumps it serviced because the bezel repair posts may crack or separate leading to inaccurate delivery of fluids to patients. The separation of one or more bezel repair posts may result in free flow of fluids to patients, fluid over delivery or under delivery, fluid interruption or power supply failure or malfunction, a [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/tenacore-recalls-alaris-pump-bezel-assembly-and-alaris-infusion-pumps-repaired-bezel-assembly-due?utm%5Fmedium=email&utm%5Fsource=govdelivery) says. The infusion pump is used to deliver fluids such as medications, nutrients, solutions, blood, and other therapies in controlled amounts. Bezel posts by Tenacore are used to service and repair infusion pump modules, the notice says.