Persona Partial Knee System Product Usage: The Persona Partial Knee… — Class II medical device recall Z-0596-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-02-21, distributed nationwide. Potential for the Persona Partial Knee Impactor Pad to fracture.
| Recall number | Z-0596-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2017-08-28 |
| Classified | 2018-02-13 |
| Reported by FDA | 2018-02-21 |
| Terminated | 2018-08-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | BE, CH, DE, ES, FR, GB, IT, JP, NL, SE |
| Quantity | 1,275 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00880304810242 |
| Lot numbers | 63517759, 63555750, 63555752, 63561883, 63561884, 63594914, 63698564, 63705328 |
| Model numbers | 42539909100 |
Product
Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to facilitate the implantation of PPK implantable components into the medical knee compartment during unicondylar knee replacement.
Reason for recall
Potential for the Persona Partial Knee Impactor Pad to fracture.
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-0596-2018. 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.