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# Class 1 Recall on Alaris Pump Syringe/PCA Modules
- URL: https://www.fdaweb.com/class-1-recall-on-alaris-pump-syringe-pca-modules/
- Published: 2020-09-16T12:00:00.000Z
- Updated: 2026-09-14T16:28:51.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5147668

FDA has classified as Class 1 a recall involving a Becton Dickinson CareFusion recall of its Alaris Syringe and Alaris PCA Modules due to potential incorrect display of syringe types and sizes. A [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/becton-dickinson-bd-carefusion-303-inc-recalls-alaristm-syringe-and-alaristm-pca-modules-due?ref=fdaweb.com) says the display errors could result in delays in infusion, under-infusion, or over-infusion, which could lead to serious adverse events, including death. The infusion pumps deliver fluids, medications, blood and blood products into a patient’s body in controlled amounts.