---
title: "Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044 — FDA record Z-0651-2022 | Is It on Recall"
description: "There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem."
url: https://isitonrecall.com/recall/fda-device-z-0651-2022-exeter-v40-cemented-hip-125mm-stem-part-number-0580-1-044/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044 — FDA record Z-0651-2022

Reported terminated

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 30, 2021. 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**: Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044
- **Reason**: There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem.
- **Classification**: Class II
- **Recalling firm**: Howmedica Osteonics Corp.
- **Quantity**: 59 devices
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0651-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0651-2022%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 | GTIN: 04546540509048; Lot G7900236 |

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

## Distribution

The product was distributed to the following US states: MI

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

- [Michigan](https://isitonrecall.com/state/michigan/)

## Dates in the source

- **Report date**: Feb 23, 2022
- **Recall initiation date**: Dec 30, 2021
- **Center classification date**: Feb 17, 2022
- **Termination date**: Mar 14, 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-0651-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Howmedica Osteonics Corp. records](https://isitonrecall.com/brand/howmedica-osteonics-corp/)