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# Class 1 Recall of Alaris Pump Module
- URL: https://www.fdaweb.com/class-1-recall-of-alaris-pump-module/
- Published: 2020-10-02T12:00:00.000Z
- Updated: 2026-09-14T16:31:15.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5147792

FDA has classified as Class 1 a recall of Becton Dickinson’s Alaris Pump Module and Pump Module Door Assembly Replacement Kits because the keypad may have one or more keys that become unresponsive or stuck. The infusion pump module delivers fluids, medications, blood and blood products into a patient’s body in controlled amounts. A [recall notice](https://lnks.gd/l/eyJhbGciOiJIUzI1NiJ9.eyJidWxsZXRpbl9saW5rX2lkIjoxMDIsInVyaSI6ImJwMjpjbGljayIsImJ1bGxldGluX2lkIjoiMjAyMDEwMDIuMjgxMzAyOTEiLCJ1cmwiOiJodHRwczovL3d3dy5mZGEuZ292L21lZGljYWwtZGV2aWNlcy9tZWRpY2FsLWRldmljZS1yZWNhbGxzL2JlY3Rvbi1kaWNraW5zb24tY2FyZWZ1c2lvbi0zMDMtaW5jLXJlY2FsbHMtYWxhcmlzdG0tc3lzdGVtLXB1bXAtbW9kdWxlLWFuZC1wdW1wLW1vZHVsZS1kb29yP3V0bV9tZWRpdW09ZW1haWwmdXRtX3NvdXJjZT1nb3ZkZWxpdmVyeSJ9.xdEXP6g6ZeGeyR9gIOqYjtBGRBeFnJER4z8W%5F%5FWSQvk/s/1255931999/br/86339899908-l?ref=fdaweb.com) says that if keys are unresponsive or stuck, this may lead to an infusion delay or prevent clinicians from changing fluid or medication infusions on the affected devices. The company has received 976 complaints about the device issue, and so far no injuries or deaths have been reported.