Stryker Neurovascular recalls Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter

Recall date

November 28, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0347-2018

FDA classification

Class II

Brand / firm

Stryker Neurovascular

Sold / distributed

OUS only - NL, FR, IT, DE, BE

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter