Drug recall
PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended for use in total hip…
FDA recall event 74752 · Class II · MicroPort Orthopedics Inc.
Key facts
| Event ID | 74752 |
|---|---|
| Recall numbers | Z-2588-2016 |
| Recalling firm | MicroPort Orthopedics Inc. |
| Product type | Devices |
| Products | PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Profemur(R) neck, Item Number PHA01222 (Short AR VV2 Ti Neck) was labeled as Item Number PHA01212 (Short AR VV1 Ti Neck). |
| Initiation date | Jun 30, 2016 |
| Report date | Aug 24, 2016 |
| Termination date | Jan 21, 2017 |
| 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: