# FDA recall Z-1509-2022

> **Corin Ltd** · Class II · device recall initiated 2022-07-22.

## Product

Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS,  Part Number 579.0103

## Reason for recall

One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.

## Distribution

US Nationwide distribution in the states of OK, TX, FL.

## Key facts

- **Recall number:** Z-1509-2022
- **Recalling firm:** Corin Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-22
- **Report date:** 2022-08-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cirencester, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1509-2022

## Citation

> AI Analytics. FDA recall Z-1509-2022. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-1509-2022. Source: US FDA. Licensed CC0.

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