Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever Recalled by Stryker Neurovascular Due to Stryker Neurovascular has become aware that at least...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Neurovascular directly.
Affected Products
Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter
Quantity: N/A
Why Was This Recalled?
Stryker Neurovascular has become aware that at least 1 (one) Trevo XP Provue System was manufactured where the carton sleeve did not match the physical contents of the pack.
Where Was This Sold?
This product was distributed to 1 state: DE
About Stryker Neurovascular
Stryker Neurovascular has 108 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report