# FDA recall Z-2610-2021

> **Corin Ltd** · Class II · device recall initiated 2021-07-28.

## Product

Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femoral Posterior Augment, REF 1122370, Sterile, a component of the Unity Total Knee System.

## Reason for recall

The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.

## Distribution

US Nationwide distribution in the states of AZ, CA, FL, IL, OK, PA, TX, UT, and WI.

## Key facts

- **Recall number:** Z-2610-2021
- **Recalling firm:** Corin Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-28
- **Report date:** 2021-10-06
- **Termination date:** 2024-06-12

- **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-2610-2021

## Citation

> AI Analytics. FDA recall Z-2610-2021. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2610-2021. Source: US FDA. Licensed CC0.

---

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