FDAClass II · Medical device · Recalled July 1, 2026

Brand Name recall — Zimmer, Inc.

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

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2578-2026
Brand: Zimmer
Classification: Class II
Units affected: 12
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

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

Affected products

Brand Name

Companies & origin

Recalling firm location: Warsaw, IN, United States
Firm address: 1800 W Center St, N/A, 46580-2304

Identifying details (verbatim from the notice)

Product codes / lots: Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947
Distribution: 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.
Firm notified the public via: Letter
FDA event ID: 99073
Recall initiated: May 11, 2026
FDA classified: June 24, 2026
FDA report date: July 1, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 24, 2026 at 12:00 AM UTC.

Report a data error on this page