Drug recall
LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00
FDA recall event 94926 · Class II · LINK BIO CORP
Key facts
| Event ID | 94926 |
|---|---|
| Recall numbers | Z-2445-2024 |
| Recalling firm | LINK BIO CORP |
| Product type | Devices |
| Products | LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down… |
| Initiation date | Jun 27, 2024 |
| Report date | Jul 31, 2024 |
| City | Dover |
| State | NJ |
| Country | United States |
| FEI number | 3016534972 |
At a glance
- 1–9 Products in this recall
- None 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: