# FDA recall Z-0273-2023

> **Corin Ltd** · Class II · device recall initiated 2022-10-31.

## Product

Unity Total Knee System.      Used for knee prosthesis in total knee replacement

## Reason for recall

The internal packaging system for devices may have damage to the blisters potentially damaging the device or compromising the sterility of the packaging.

## Distribution

Distribution in the US to New Jersy and Puerto Rico.  International distribution to South Africa and France.

## Key facts

- **Recall number:** Z-0273-2023
- **Recalling firm:** Corin Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-10-31
- **Report date:** 2022-11-30
- **Termination date:** 2024-01-12

- **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-0273-2023

## Citation

> AI Analytics. FDA recall Z-0273-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0273-2023. Source: US FDA. Licensed CC0.

---

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