---
title: "MobileLink Acetabular Cup System, Shell/Insert Adapter for Shell 74-80mm, Ins... — FDA record Z-2641-2023 | Is It on Recall"
description: "Product is labeled with incorrect offset."
url: https://isitonrecall.com/recall/fda-device-z-2641-2023-mobilelink-acetabular-cup-system-shell-insert-adapter-for-shell-74-80mm-insert-size-f-12mm-offset-20/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# MobileLink Acetabular Cup System, Shell/Insert Adapter for Shell 74-80mm, Insert Size F, +12mm Offset 20 degrees Incl... — FDA record Z-2641-2023

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 Jul 14, 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**: MobileLink Acetabular Cup System, Shell/Insert Adapter for Shell 74-80mm, Insert Size F, +12mm Offset 20 degrees Inclination
- **Reason**: Product is labeled with incorrect offset.
- **Classification**: Class II
- **Recalling firm**: Waldemar Link GmbH & Co. KG (Mfg Site)
- **Quantity**: 8 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2641-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2641-2023%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: 04026575182329 Item Number: 183-610/05 Lots: 210526/0781; 210526/0777; 210526/0779; 210526/0771; 210526/0772; 210526/0783; 210526/0784; 210526/0778 |

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

## Distribution

Domestic distribution to AL, NJ, NV.

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

- [Alabama](https://isitonrecall.com/state/alabama/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Nevada](https://isitonrecall.com/state/nevada/)

## Dates in the source

- **Report date**: Oct 4, 2023
- **Recall initiation date**: Jul 14, 2023
- **Center classification date**: Sep 26, 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-2641-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Waldemar Link GmbH & Co. KG (Mfg Site) records](https://isitonrecall.com/brand/waldemar-link-gmbh-co-kg-mfg-site/)