Medtronic Recalls Valiant Navion Thoracic Stent Graft System Due to Risk of Stent Fractures and Type III Endoleaks
By: Aorn Staff
Published: 12/31/2021
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April 9, 2021
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Recalled Product
- Medtronic Valiant Navion Thoracic Stent Graft System
- Model Number, Product Codes, Catalog or Lot numbers: Please See Links Below.
- Distribution Dates: November 12, 2018 to February 10, 2021
- Devices Recalled in the U.S.: 14,237
- Date Initiated by Firm: February 4, 2021
