Unity Total Knee System — Class II medical device recall Z-0273-2023
Terminated recall by Corin Ltd, reported 2022-11-30, distributed in PR. The internal packaging system for devices may have damage to the blisters potentially damaging the device or c
| Recall number | Z-0273-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Corin Ltd, Cirencester, N/A, United Kingdom |
| Recall initiated | 2022-10-31 |
| Classified | 2022-11-21 |
| Reported by FDA | 2022-11-30 |
| Terminated | 2024-01-12 |
| Distributed | PR |
| Countries outside the US | FR, ZA |
| Quantity | 4 devices |
| Reason classes | sterility |
| Lot numbers | 504337 |
| Model numbers | 112.040.06 |
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.
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-0273-2023. 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.