Drug recall
Medtronic ENT Ultra Round Steel Cutting Bur, Model Number REF 31313069
FDA recall event 95162 · Class II · Medtronic Xomed, Inc.
Key facts
| Event ID | 95162 |
|---|---|
| Recall numbers | Z-3130-2024 |
| Recalling firm | Medtronic Xomed, Inc. |
| Product type | Devices |
| Products | Medtronic ENT Ultra Round Steel Cutting Bur, Model Number REF 31313069 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product was distributed past expiration date. |
| Initiation date | Jul 5, 2024 |
| Report date | Sep 18, 2024 |
| City | Jacksonville |
| State | FL |
| Country | United States |
| FEI number | 1045254 |
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: