PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK — Class II medical device recall Z-1225-2022
Terminated recall by MicroPort Orthopedics Inc., reported 2022-06-08, distributed nationwide. One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.
| Recall number | Z-1225-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MicroPort Orthopedics Inc., Arlington, TN, United States |
| Recall initiated | 2022-05-04 |
| Classified | 2022-06-02 |
| Reported by FDA | 2022-06-08 |
| Terminated | 2024-01-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 8 units |
| UPC / GTIN / UDI-DI | 00192629112773 |
| Lot numbers | 1903727 |
| Model numbers | 00192629112773, 1903727, PHAPCLS7 |
| Expiration dates | 2029-11-24 |
Product
PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
Reason for recall
One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.
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-1225-2022. 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.