Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
FDA Recall #Z-0392-2022 — Class II — December 3, 2021
Product Description
Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
Reason for Recall
The incorrect product is contained in the packaging.
Recalling Firm
Wright Medical Technology Inc — Arlington, TN
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
23 units
Distribution
Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom.
Code Information
Lot #1642103
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated