Corin Unity Knee Augments — Class II medical device recall Z-2610-2021
Terminated recall by Corin Ltd, reported 2021-10-06, distributed nationwide. The packaging system on the devices have potential physical and water damage resulting in damage to the device
| Recall number | Z-2610-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Corin Ltd, Cirencester, N/A, United Kingdom |
| Recall initiated | 2021-07-28 |
| Classified | 2021-09-30 |
| Reported by FDA | 2021-10-06 |
| Terminated | 2024-06-12 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
| Reason classes | sterility |
| Lot numbers | 472687 |
| Model numbers | 1122370 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2610-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.