Official recall notice
FDA DeviceClass IINotable
FDA Recall: Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augme
- Recall date
- 2026-07-01
- Brand
- Zimmer, Inc.
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
Product description
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
Affected products
Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947