Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless — Class II medical device recall Z-2365-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-07-11.
| Recall number | Z-2365-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2018-05-30 |
| Classified | 2018-07-05 |
| Reported by FDA | 2018-07-11 |
| Terminated | 2020-05-28 |
| Countries outside the US | JP |
| Quantity | 24 |
Product
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 10; 00-7713-010-00
Reason for recall
Not stated by FDA.
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-2365-2018. 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.