Recall Ledger

Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿... recall (Zimmer, Inc.)

Medical deviceClass IIOngoing

Summary: Zimmer, Inc. is recalling Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Size 9, 9+ 10mm Thicknes Component: N/A. Reason: Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.

What is being recalled

Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Size 9, 9+ 10mm Thicknes Component: N/A

Why

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

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

Refer to the attached ZFA 2026-00088_Initial Consignee List and ZFA 2026-00088_Initial Distribution History containing the distribution and the identification of the affected consignees.

How to tell if yours is affected

Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-2578-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedMay 11, 2026
ReportedJuly 1, 2026
CompanyZimmer, Inc.
Company locationWarsaw, IN, United States
Initiated byVoluntary: Firm initiated
Quantity12

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Official FDA record