---
title: "Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal... — FDA record Z-2578-2026 | Is It on Recall"
description: "Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package."
url: https://isitonrecall.com/recall/fda-device-z-2578-2026-brand-name-persona-revision-product-name-persona-revision-trabecular-metal-femoral-distal-augment-mo/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog N... — FDA record Z-2578-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 11, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
- **Classification**: Class II
- **Recalling firm**: Zimmer, Inc.
- **Quantity**: 12
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2578-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2578-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947 |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jul 1, 2026
- **Recall initiation date**: May 11, 2026
- **Center classification date**: Jun 24, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2578-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Zimmer, Inc. records](https://isitonrecall.com/brand/zimmer-inc/)