stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
Reported: May 3, 2023 Initiated: April 10, 2023 #Z-1467-2023
Product Description
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
Reason for Recall
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
Details
- Recalling Firm
- Wright Medical Technology, Inc.
- Units Affected
- 50 units
- Distribution
- US Nationwide distribution.
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation. Recalled by Wright Medical Technology, Inc.. Units affected: 50 units.
Why was this product recalled? ▼
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 3, 2023. Severity: Moderate. Recall number: Z-1467-2023.
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