Wright Medical Technology, Inc. recalls stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
- Recall date
- April 10, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1466-2023
- FDA classification
- Class II
- Brand / firm
- Wright Medical Technology, Inc.
- Sold / distributed
- US Nationwide distribution.
Why it was recalled
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
Get recall alerts
Free email alert whenever Wright Medical Technology, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Wright Medical Technology, Inc.