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Recall notifications
For questions pertaining to a specific medical device recall, please see the contact information within the product recall notice or customer letter.
Recall Notification - BD Nexiva™ Closed IV Catheter System – Dual Port (20 GA 1.75 IN)
Sep 14, 2020
BD Nexiva™ Closed IV Catheter System – Dual Port (20 GA 1.75 IN)
Recall Notification - BD Alaris™ PC Unit Model 8015
Aug 4, 2020
BD is initiating a voluntary recall for the BD Alaris™ PC Unit Model 8015 to inform you that the PC unit keypad may exhibit unresponsive or stuck keys as a result of fluid ingress potentially resulting in a delay to the start of infusion or interruption of infusion.
Recall Notification - BD Alaris™ Pump Module Model 8100
Aug 4, 2020
BD is initiating a voluntary recall for the BD Alaris™ Pump Module Model 8100 to inform you that the keypad may exhibit unresponsive or stuck keys as a result of fluid ingress.
Recall Notification - BD Alaris™ Syringe Module Model 8110 and PCA Module Model 8120
Aug 4, 2020
BD is initiating a voluntary recall for the Alaris™ Syringe Module and Alaris™ PCA Module to inform you of the potential for the Alaris PC unit to display incorrect syringe types and/or syringe sizes.
Recall notification - BD Alaris™ EtCO2 Module model 8300 channel error
Aug 4, 2020
BD is initiating a voluntary recall for the Alaris™ EtCO2 Module to inform you of an issue with a component within the EtCO2 Module that may result in a channel error.