---
title: "EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706 — FDA record Z-0761-2025 | Is It on Recall"
description: "Knee insert package may contain an acetabular system, which may cause surgical delay to get a new product."
url: https://isitonrecall.com/recall/fda-device-z-0761-2025-empowr-3d-knee-tibial-insert-6r-10mm-ve-ref-342-10-706/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706 — FDA record Z-0761-2025

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 Dec 10, 2024. 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**: EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706
- **Reason**: Knee insert package may contain an acetabular system, which may cause surgical delay to get a new product.
- **Classification**: Class II
- **Recalling firm**: Encore Medical, LP
- **Quantity**: 9
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0761-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0761-2025%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 | UDI-DI: 00888912167338. Lot: 076T1273A |

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

## Distribution

US Nationwide distribution in the states of IN, KS, CA, FL, NY, TX, AL, WA.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Georgia](https://isitonrecall.com/state/georgia/)
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- [North Dakota](https://isitonrecall.com/state/north-dakota/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)
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- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)
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- [Wisconsin](https://isitonrecall.com/state/wisconsin/)
- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jan 1, 2025
- **Recall initiation date**: Dec 10, 2024
- **Center classification date**: Dec 23, 2024

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-0761-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Encore Medical, LP records](https://isitonrecall.com/brand/encore-medical-lp/)