Wright Medical Technology, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1466-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 10, 2023

Date Posted: May 3, 2023

Recall Number: Z-1466-2023

Event ID: 92078

Reason for Recall:

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

Status: Ongoing

Product Quantity: 41 units

Code Information:

UDI/DI 00889797101011, Lot Number 1736809

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated