EVOLUTION MP Tibial Bases — Class II medical device recall Z-0275-2023
Terminated recall by MicroPort Orthopedics Inc., reported 2023-02-22. One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opene
| Recall number | Z-0275-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MicroPort Orthopedics Inc., Arlington, TN, United States |
| Recall initiated | 2022-10-28 |
| Classified | 2022-11-22 |
| Reported by FDA | 2023-02-22 |
| Terminated | 2026-09-10 |
| Countries outside the US | AT, BE, CN, DE, FR, GR, IT, JP, RO |
| Quantity | 24 units |
| Lot numbers | 1916559 |
| Model numbers | ETPKN2PL |
Product
EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial base
Reason for recall
One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in 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-0275-2023. 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.