FDA DeviceClass IINotable

FDA Recall: Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augme

Date: 2026-07-01
Brand: Zimmer, Inc.
Category: Medical Device
FDA Class: Class II

Description

Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.

Hazard

Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.

Remedy

12

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