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# FDA Classifies 4 Recent BD Alaris Pump Recalls
- URL: https://www.fdaweb.com/fda-classifies-4-recent-bd-alaris-pump-recalls/
- Published: 2020-09-21T12:00:00.000Z
- Updated: 2026-09-14T16:29:21.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5147692

Becton, Dickinson says four previously announced recalls of its BD Alaris System have been classified as follows:

1. [Alaris PC Unit Model 8015 Front Case with Keypad Replacement Kits](https://c212.net/c/link/?t=0&l=en&o=2921181-1&h=517250602&u=https%3A%2F%2Fwww.bd.com%2Fen-us%2Fsupport%2Frecall-notifications%2Frecall-notification-bd-alaris-pc-unit-model-8015&a=Alaris+PC+Unit+Model+8015+Front+Case+with+Keypad+Replacement+Kits&ref=fdaweb.com) (Class 1 recall): The pump module keypad may exhibit keys that are unresponsive or stuck as a result of fluid ingress, potentially resulting in a delay to the start of infusion, interruption of infusion or inability to titrate medication.
2. [Alaris Pump Module Model 8100 Front Case with Keypad Replacement Kits](https://c212.net/c/link/?t=0&l=en&o=2921181-1&h=1267609958&u=https%3A%2F%2Fwww.bd.com%2Fen-us%2Fsupport%2Frecall-notifications%2Frecall-notification-bd-alaris-pc-unit-model-8100&a=Alaris+Pump+Module+Model+8100+Front+Case+with+Keypad+Replacement+Kits&ref=fdaweb.com) (Class 1 recall): Pump module keypad may exhibit keys that are unresponsive or stuck as a result of fluid ingress, potentially resulting in a delay to the start of infusion or interruption of infusion.
3. [BD Alaris Syringe Module Model 8110 and PCA Module Model 8120](https://c212.net/c/link/?t=0&l=en&o=2921181-1&h=1046569586&u=https%3A%2F%2Fwww.bd.com%2Fen-us%2Fsupport%2Frecall-notifications%2Frecall-notification-bd-alaris-syringe-module-model-8110-and-pca-module-model-8120&a=BD+Alaris%E2%84%A2+Syringe+Module+Model+8110+and+PCA+Module+Model+8120&ref=fdaweb.com) (Class 1 recall: The Alaris PC unit may display incorrect syringe type or syringe sizes. This could potentially result in delays in infusion, under-infusion or over-infusion.
4. [BD Alaris EtCO2 Module model 8300 channel error](https://c212.net/c/link/?t=0&l=en&o=2921181-1&h=357703732&u=https%3A%2F%2Fwww.bd.com%2Fen-us%2Fsupport%2Frecall-notifications%2Frecall-notification-bd-alaris-etco2-module-model-8300-channel-error&a=BD+Alaris%E2%84%A2+EtCO2+Module+model+8300+channel+error&ref=fdaweb.com) (Class 2 recall) Infusion pump component defect may result in interruption of patient monitoring.

The recalls were announced by the company in August.