# FDA recall Z-2517-2018

> **IMPLANTCAST GMBH** · Class II · device recall initiated 2017-12-28.

## Product

2M insert 15degree for MUTARS RS cup and LUMiC TiN orthopedic hip implant acetabular component.    Size 38/39 mm REF number 02423839   Size 42/44 mm REF number 02424244    Size 44/48 mm REF number 02424448    Size 46/52 mm REF number 02424652

## Reason for recall

Possibility that the retaining ring in the 2M inlay 15degree for MUTARS RS Cup and LUMiC TiN is incorrectly mounted.

## Distribution

Distribution in Europe and US states of Texas, Rhode Island and Georgia.

## Key facts

- **Recall number:** Z-2517-2018
- **Recalling firm:** IMPLANTCAST GMBH
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-28
- **Report date:** 2018-08-01
- **Termination date:** 2020-09-01

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2517-2018

## Citation

> AI Analytics. FDA recall Z-2517-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2517-2018. Source: US FDA. Licensed CC0.

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