Z-0347-2018 Class II Terminated

Recalled by Stryker Neurovascular — Fremont, CA

Recall Details

Product Type
Devices
Report Date
January 24, 2018
Initiation Date
November 28, 2017
Termination Date
April 28, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
N/A

Product Description

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

Reason for Recall

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.

Distribution Pattern

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

Code Information

UPN/Model No. 80052; Lot 63034