---
title: "Exeter V40 Trial Head, 26mm, -3, Catalog Number 6364-8-026 — FDA record Z-1921-2023 | Is It on Recall"
description: "The Exeter V40 Trial Head, catalog number 6364-8-026 (size 26mm, -3) may appear green, when it is meant to be a blue color. Green signifies a size 26mm, +3 Tria"
url: https://isitonrecall.com/recall/fda-device-z-1921-2023-exeter-v40-trial-head-26mm-3-catalog-number-6364-8-026/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Exeter V40 Trial Head, 26mm, -3, Catalog Number 6364-8-026 — FDA record Z-1921-2023

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 May 3, 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**: Exeter V40 Trial Head, 26mm, -3, Catalog Number 6364-8-026
- **Reason**: The Exeter V40 Trial Head, catalog number 6364-8-026 (size 26mm, -3) may appear green, when it is meant to be a blue color. Green signifies a size 26mm, +3 Trial Head.
- **Classification**: Class II
- **Recalling firm**: Howmedica Osteonics Corp.
- **Quantity**: 2 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1921-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1921-2023%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: 07613327188660; Lot Number: G7207242 |

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

## Distribution

International distribution in the country of Ireland.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jun 21, 2023
- **Recall initiation date**: May 3, 2023
- **Center classification date**: Jun 14, 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-1921-2023%22)

## Related records

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