Brand Name: Persona Revision Product Name: Persona Revision¿… — Class II medical device recall Z-2578-2026
Ongoing recall by Zimmer, Inc., reported 2026-07-01. Firm received a complaint with no clinical impact in which a posterior augment was found within the distal aug
| Recall number | Z-2578-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2026-05-11 |
| Classified | 2026-06-24 |
| Reported by FDA | 2026-07-01 |
| Quantity | 12 |
| UPC / GTIN / UDI-DI | 00889024561014 |
| Lot numbers | 66232947 |
| Model numbers | 42-5572-066-10 |
Product
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 for recall
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2578-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.