Stryker Corporation recalls 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is design…

Recall date

December 21, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2057-2018

FDA classification

Class II

Brand / firm

Stryker Corporation

Sold / distributed

US distribution to Massachusetts only..

Why it was recalled

Inadvertent shipment of expired units.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.