Drug recall
PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
FDA recall event 90140 · Class II · MicroPort Orthopedics Inc.
Key facts
| Event ID | 90140 |
|---|---|
| Recall numbers | Z-1225-2022 |
| Recalling firm | MicroPort Orthopedics Inc. |
| Product type | Devices |
| Products | PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body. |
| Initiation date | May 4, 2022 |
| Report date | Jun 8, 2022 |
| Termination date | Jan 16, 2024 |
| City | Arlington |
| State | TN |
| Country | United States |
| FEI number | 3010536692 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: