# FDA recall Z-2641-2023

> **Waldemar Link GmbH & Co. KG (Mfg Site)** · Class II · device recall initiated 2023-07-14.

## Product

MobileLink Acetabular Cup System, Shell/Insert Adapter for Shell 74-80mm, Insert Size F, +12mm Offset 20 degrees Inclination

## Reason for recall

Product is labeled with incorrect offset.

## Distribution

Domestic distribution to AL, NJ, NV.

## Key facts

- **Recall number:** Z-2641-2023
- **Recalling firm:** Waldemar Link GmbH & Co. KG (Mfg Site)
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-07-14
- **Report date:** 2023-10-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Norderstedt, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2641-2023

## Citation

> AI Analytics. FDA recall Z-2641-2023. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-2641-2023. Source: US FDA. Licensed CC0.

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