3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable...
FDA Recall #Z-2057-2018 — Class II — December 21, 2017
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.
Reason for Recall
Inadvertent shipment of expired units.
Recalling Firm
Stryker Corporation — San Jose, CA
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
2 boxes (5 units per box)
Distribution
US distribution to Massachusetts only..
Code Information
Lot No. 14239AG2, UPC 07613327055795. The expiration date marked on the box is August 2018, but it should be August 2016.
Status
Completed
Voluntary / Mandated
Voluntary: Firm initiated