---
title: "ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Co... — FDA record Z-1456-2024 | Is It on Recall"
description: "Product incorrectly labelled."
url: https://isitonrecall.com/recall/fda-device-z-1456-2024-attune-affixium-cementless-fixed-bearing-knee-with-3dp-technology-size-6-component-of-the-attune-tot/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Component of the ATTUNE Total Knee Replace... — FDA record Z-1456-2024

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 Mar 12, 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**: ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Component of the ATTUNE Total Knee Replacement System.
- **Reason**: Product incorrectly labelled.
- **Classification**: Class II
- **Recalling firm**: DePuy Orthopaedics, Inc.
- **Quantity**: 5 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1456-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1456-2024%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 | Model No: 150621006; UDI-DI: 10603295507451; Lot JA06A0252. |

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

## Distribution

Worldwide - US Nationwide distribution in the states of CA, IL, NJ, WI and the country of Canada.

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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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Apr 10, 2024
- **Recall initiation date**: Mar 12, 2024
- **Center classification date**: Mar 29, 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-1456-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [DePuy Orthopaedics, Inc. records](https://isitonrecall.com/brand/depuy-orthopaedics-inc/)