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# CareFusion Recalls Alaris Pump Module
- URL: https://www.fdaweb.com/carefusion-recalls-alaris-pump-module/
- Published: 2023-11-08T12:00:00.000Z
- Updated: 2026-09-14T14:15:38.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5155747

Becton Dickinson’s CareFusion unit has recalled (Class 1) its Alaris Patient Controlled Analgesia infusion pump module 8120 because the compatible syringes’ labeling contains syringes that have not been validated. In a recent letter to users, the company told them to stop using certain Cardinal Health-branded Monoject syringes with the BD Alaris Syringe and PCA Modules, according to a [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=203462&ref=fdaweb.com). It also included a listing of the syringes that are compatible with the device and its modules.