Stryker Neurovascular: Medical Device Recall in 2018 - (Recall #: Z-3020-2018)

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:

Wingspan Stent System, Rx Only, Sterile EO, Catalog #: M003WE0250090, M003WE0300090, M003WE0350090, M003WE0400090, M003WE0450090, M003WE0250150, M003WE0300150, M003WE0350150, M003WE0400150, M003WE0450150, M003WE0250200, M003WE0300200, M003WE0350200, M003WE0400200, M003WE0450200

Product Classification:

Class II

Date Initiated: June 5, 2018

Date Posted: September 19, 2018

Recall Number: Z-3020-2018

Event ID: 80204

Reason for Recall:

Use-related coating damage on delivery catheter shafts of Wingspan delivery catheters were reported

Status: Terminated

Product Quantity: 11585

Code Information:

All lots.

Distribution Pattern:

China

Voluntary or Mandated:

Voluntary: Firm initiated