# FDA recall Z-2578-2026

> **Zimmer, Inc.** · Class II · device recall initiated 2026-05-11.

## 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.

## 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.

## Key facts

- **Recall number:** Z-2578-2026
- **Recalling firm:** Zimmer, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-11
- **Report date:** 2026-07-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2578-2026

## Citation

> MORVS. FDA recall Z-2578-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2578-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*