Class II — MicroPort Orthopedics Inc.
| Recalling firm | MicroPort Orthopedics Inc. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body. |
| Product | PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK |
| Quantity | 8 units |
| Distribution | Worldwide distribution - US Nationwide distribution in the states of FL, IN, MO, CA and the country of Canada. |
| Initiated | 2022-05-04 |
| Classified | 2022-06-02 |
| Terminated | 2024-01-16 |
| Recall number | Z-1225-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — MicroPort Orthopedics Inc. (Z-1225-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90140/
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