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# Baxter Spectrum Pump Recall is Class 1
- URL: https://www.fdaweb.com/baxter-spectrum-pump-recall-is-class-1/
- Published: 2025-03-20T12:00:00.000Z
- Updated: 2026-09-14T14:55:51.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5158862

FDA says the Baxter 2/5 recall of certain Spectrum infusion pumps is Class 1\. An updated medical device early alert [says](https://www.google.com/url?sa=t&source=web&rct=j&opi=89978449&url=https://www.fda.gov/medical-devices/medical-device-recalls/update-alert-infusion-pump-issue-baxter-healthcare-corporation&ved=2ahUKEwiNtKb4o5mMAxVdF1kFHa2OHFkQvOMEKAB6BAgXEAE&usg=AOvVaw02dJQyQoRPdtOoEU2CxEGK) the pumps were recalled due to the potential for missing motor mounting screws, which may have occurred during the servicing process. The company said the affected pumps should be returned for inspection and reservicing as applicable.

Baxter reported one serious injury related to the issue, FDA says.