---
title: "PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610 — FDA record Z-0524-2024 | Is It on Recall"
description: "Due to incorrect product labeling"
url: https://isitonrecall.com/recall/fda-device-z-0524-2024-physica-hps-tibial-liner-6-h10-ref-6539-54-610/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610 — FDA record Z-0524-2024

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 27, 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**: PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610
- **Reason**: Due to incorrect product labeling
- **Classification**: Class II
- **Recalling firm**: Limacorporate S.p.A
- **Quantity**: 33 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0524-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0524-2024%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 | Product Code: 6539.54.610 UDI-DI Code: 08033390212786 Lot/Sterilization Numbers: 2122621 / 2200149 2203871 / 2200167 |

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

## Distribution

U.S Distribution: AZ, CA, IL, LA, and NY

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

- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [New York](https://isitonrecall.com/state/new-york/)

## Dates in the source

- **Report date**: Dec 20, 2023
- **Recall initiation date**: Oct 27, 2023
- **Center classification date**: Dec 9, 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-0524-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Limacorporate S.p.A records](https://isitonrecall.com/brand/limacorporate-s-p-a/)