Stryker Neurovascular: Medical Device Recall in 2017 - (Recall #: Z-0277-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Trevo(TM) XP ProVue Procedure Pack, TREVO(TM) XP PROVUE RETRIEVER, 6 mm, 25 mm, .Excelsior(TM) XT-27(TM) 1 TIP STRAIGHT, 150 cm, 6 cm, Microcatheter; UPN 93068 Stroke intervention kit

Product Classification:

Class II

Date Initiated: November 3, 2017

Date Posted: December 27, 2017

Recall Number: Z-0277-2018

Event ID: 78607

Reason for Recall:

Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs and Trevo Procedure Packs were manufactured using a carton sleeve where the sleeve label contents did not match the physical contents within the pack.

Status: Terminated

Product Quantity: 1 unit

Code Information:

Lot Number QX10100894. Exp. Date 28-Oct-18

Distribution Pattern:

International Distribution to: Germany, Slovakia and Israel.

Voluntary or Mandated:

Voluntary: Firm initiated