Stryker Corporation: Medical Device Recall in 2018 - (Recall #: Z-2057-2018)

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:

3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of entry for arthroscopic instruments into the joints.

Product Classification:

Class II

Date Initiated: December 21, 2017

Date Posted: June 13, 2018

Recall Number: Z-2057-2018

Event ID: 79978

Reason for Recall:

Inadvertent shipment of expired units.

Status: Completed

Product Quantity: 2 boxes (5 units per box)

Code Information:

Lot No. 14239AG2, UPC 07613327055795. The expiration date marked on the box is August 2018, but it should be August 2016.

Distribution Pattern:

US distribution to Massachusetts only..

Voluntary or Mandated:

Voluntary: Firm initiated