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# Baxter Clearlink Solution Set Recall is Class 1
- URL: https://www.fdaweb.com/baxter-clearlink-solution-set-recall-is-class-1/
- Published: 2022-09-15T12:00:00.000Z
- Updated: 2026-09-14T17:59:27.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5152745

FDA says the Baxter Healthcare 8/9 recall of 511,728 Clearlink Basic Solution Sets with Duovent is Class 1\. An agency [notice](https://www.fda.gov/medical-devices/medical-device-recalls/baxter-healthcare-corporation-recalls-clearlink-basic-solution-set-duovent-risk-leaks-may-expose?ref=fdaweb.com) says the devices, which are used as part of a system to administer drugs and solutions to patients, were recalled after increased consumer reports of leaks. The sets were distributed between 10/14/20 and 6/30/22.

FDA says there have been 83 complaints associated with the issue, with no reports of injuries or deaths.