Stryker Neurovascular: Medical Device Recall in 2017 - (Recall #: Z-2800-2017)

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 XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK42022001

Product Classification:

Class II

Date Initiated: June 26, 2017

Date Posted: August 9, 2017

Recall Number: Z-2800-2017

Event ID: 77671

Reason for Recall:

Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs were manufactured using a carton sleeve where the pre-printed contents on the back of the sleeve did not match the physical contents of the pack.

Status: Terminated

Product Quantity: 63 packs

Code Information:

Lot Numbers: QPC30107530, QPC30107745, QPC30107814, QPC30110247

Distribution Pattern:

nationwide

Voluntary or Mandated:

Voluntary: Firm initiated