Product Safety Recalls

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Wright Medical Technology, Inc. Recall 92078

Description: stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation

Wright Medical Technology, Inc. Recall 92078 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1467-2023
Event ID92078
Event Descriptionstryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
Product TypeDevices
DistributionUS Nationwide distribution.
Quantity50 units
Recall ReasonTwo lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
Device Classification20230503
Device Code InfoUDI/DI 00889797101035, Lot Number 1737413
Center Classification Date20230426
Recall Initiation Date20230410
Recalling FirmWright Medical Technology, Inc.
Initial Notification E-Mail
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