---
title: "G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Nu... — FDA record Z-1284-2023 | Is It on Recall"
description: "The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner."
url: https://isitonrecall.com/recall/fda-device-z-1284-2023-g7-acetabular-system-dual-mobility-acetabular-liner-40-mm-size-d-model-number-110024462/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462 — FDA record Z-1284-2023

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 Feb 6, 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**: G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
- **Reason**: The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
- **Classification**: Class II
- **Recalling firm**: Biomet, Inc.
- **Quantity**: 12 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1284-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1284-2023%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: (01)00880304703506(17)321128(10)65731960; Lot Number: 65731960 |

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

## Distribution

US Distribution to states of: AZ, FL, GA, MI, NE, and TX.

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/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Mar 29, 2023
- **Recall initiation date**: Feb 6, 2023
- **Center classification date**: Mar 23, 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-1284-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Biomet, Inc. records](https://isitonrecall.com/brand/biomet-inc/)