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# Cordis Class 1 Recall of Precise Carotid System
- URL: https://www.fdaweb.com/cordis-class-1-recall-of-precise-carotid-system/
- Published: 2021-04-23T12:00:00.000Z
- Updated: 2026-09-14T16:56:02.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149180

**Cordis has recalled (Class 1) its Precise PRO Rx Carotid System because of the potential for the distal tip to become separated from the lumen wire in specific lots. FDA** [**says**](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=185850&ref=fdaweb.com) **about 7,300 devices are affected, and so far seven reported complaints about the defect have been received, including five injuries and no deaths. The device is intended for treating** narrowed carotid arteries.