Z-1466-2023 Class II Ongoing

Recalled by Wright Medical Technology, Inc. — Memphis, TN

Recall Details

Product Type
Devices
Report Date
May 3, 2023
Initiation Date
April 10, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
41 units

Product Description

stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation

Reason for Recall

Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.

Distribution Pattern

US Nationwide distribution.

Code Information

UDI/DI 00889797101011, Lot Number 1736809