---
title: "Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision to... — FDA record Z-0213-2024 | Is It on Recall"
description: "Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa."
url: https://isitonrecall.com/recall/fda-device-z-0213-2024-unity-cr-femur-right-size-6-model-number-112-001-32-primary-and-revision-total-knee-arthroplasty/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arthroplasty — FDA record Z-0213-2024

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 Oct 13, 2023. 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**: Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arthroplasty
- **Reason**: Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa.
- **Classification**: Class II
- **Recalling firm**: Corin Ltd
- **Quantity**: 3 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0213-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0213-2024%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: (05055343872499, Lot Number: 529803. |

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

## Distribution

US: MI, TX, IL

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

- [Illinois](https://isitonrecall.com/state/illinois/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Nov 8, 2023
- **Recall initiation date**: Oct 13, 2023
- **Center classification date**: Nov 2, 2023

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-0213-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Corin Ltd records](https://isitonrecall.com/brand/corin-ltd/)