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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
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 23, 2026 at 11:04 PM UTC.
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