Get the free FDA Issues Notice of Class 2 Recall for Zimmer Persona ...
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January 22, 2015,
To:Risk Managers and SurgeonsSubject:URGENT MEDICAL DEVICE RECALLED SPECIFICAffected Product: Persona Tibial Articular Surface Inserter (Instrument)
Catalog Number: 42529900100
Zimmer
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FDA issues notice of new regulations or safety concerns.
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