Stryker Neurovascular: Medical Device Recall in 2017 - (Recall #: Z-0276-2018)

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:

Stroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 4 mm, 20 mm, ; Trevo(TM) Pro 18, TREVO PRO 18 MICROCATHETER, 0.021 in ID, 150 cm; AXS Catalyst(TM) 6, Distal Access Catheter, 0.060 in, 132 cm; UPN M0033PK42022002 Stroke intervention kit

Product Classification:

Class II

Date Initiated: November 3, 2017

Date Posted: December 27, 2017

Recall Number: Z-0276-2018

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: 2 units

Code Information:

Lot Number QPC30200039, Exp. Date 28-Aug-18; QPC30200114, Exp. Date 28-Mar18

Distribution Pattern:

International Distribution to: Germany, Slovakia and Israel.

Voluntary or Mandated:

Voluntary: Firm initiated