Stryker Neurovascular: Medical Device Recall in 2018 - (Recall #: Z-0347-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 28, 2017

Date Posted: January 24, 2018

Recall Number: Z-0347-2018

Event ID: 78716

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.

Status: Terminated

Product Quantity: N/A

Code Information:

UPN/Model No. 80052; Lot 63034

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated