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Wright Medical Technology, Inc. recalls stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
Recalled May 3, 2023 · FDA recall Z-1466-2023 · Wright Medical Technology
Hazard
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts. · FDA Class II
Units
41 units
Sold at
US Nationwide distribution.
Description
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
Product
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
Manufacturer(s)
Wright Medical Technology, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →