# FDA recall Z-0213-2024

> **Corin Ltd** · Class II · device recall initiated 2023-10-13.

## Product

Unity CR Femur Right, Size 6, Model Number 112.001.32      Primary and revision total knee arthroplasty

## Reason for recall

Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa.

## Distribution

US: MI, TX, IL

## Key facts

- **Recall number:** Z-0213-2024
- **Recalling firm:** Corin Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-13
- **Report date:** 2023-11-08

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0213-2024

## Citation

> AI Analytics. FDA recall Z-0213-2024. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0213-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*