Persona Partial Knee Spacer Blocks To assist in partial knee… — Class II medical device recall Z-1240-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-04-04, distributed nationwide. Zimmer Biomet is conducting a medical device recall for the Persona Partial Knee Spacer Blocks in sizes 8mm, 9
| Recall number | Z-1240-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2017-10-24 |
| Classified | 2018-03-28 |
| Reported by FDA | 2018-04-04 |
| Terminated | 2019-04-03 |
| Distributed | Nationwide (US) |
| Quantity | 430 |
| Lot numbers | 63547276, 63549084, 63549096, 63549097, 63552644, 63579568, 63579569, 63579674, 63579676, 63579680, 63594433, 63594434, 63596547, 63610265, 63610266, 63610267, 63613101 |
Product
Persona Partial Knee Spacer Blocks To assist in partial knee arthroplasty surgery
Reason for recall
Zimmer Biomet is conducting a medical device recall for the Persona Partial Knee Spacer Blocks in sizes 8mm, 9mm, 10mm, 12mm, and 14mm. Complaints received indicated that flexion has the potential to feel tight during range-of-motion trialing and that the final trial has the potential to appear looser in extension.
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-1240-2018. 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.