Stryker, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1084-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm

Product Classification:

Class II

Date Initiated: December 6, 2023

Date Posted: February 21, 2024

Recall Number: Z-1084-2024

Event ID: 93678

Reason for Recall:

The microcatheter IFU contains an intended use that has not been evaluated by the FDA.

Status: Ongoing

Product Quantity: 11 units

Code Information:

UDI: (01)00815742002386/Lot Number(s): 0000228865 0000370674

Distribution Pattern:

US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.

Voluntary or Mandated:

Voluntary: Firm initiated