Updated Guidance On The Management Of The Recalled Endologix Nellix Endovascular Aneurysm Sealing (evas) System (dsi/2025/004)
Recall Summary The Endologix Nellix EndoVascular Aneurysm Sealing (EVAS) System has been recalled in the UK. This device is used to treat abdominal aortic aneurysms. The UK health authorities have updated their guidance on how to manage patients who already have this device implanted.
- Reason
- The MHRA provides an update to previous guidance on the management of patients treated with the recalled Endologix Nellix EVAS System to reflect revised recommendations. All implanted patients in the UK with this device should be identified and appropriate action taken.
- Classification
- Unclassified
- Category
- drug recall
- Country
- United Kingdom
- Agency
- UK Medicines and Healthcare products Regulatory Agency
- Recall date
- 2025-07-28
- Status
- Ongoing
- Distribution
- United Kingdom
Official recall notice from UK Medicines and Healthcare products Regulatory Agency
Recall details on Nibble Recalls: https://trynibble.app/recalls/070387a0-90b2-494b-bb7f-24247107f0c7