Drug recall
SenSight Connector Plug, Model Number B31061.
FDA recall event 93083 · Class II · Medtronic Neuromodulation
Key facts
| Event ID | 93083 |
|---|---|
| Recall numbers | Z-0121-2024 |
| Recalling firm | Medtronic Neuromodulation |
| Product type | Devices |
| Products | SenSight Connector Plug, Model Number B31061. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Medtronic is requesting return of a small number of units of the SenSight Connector Plug, Model B31061, due to a discrepancy in the Use By Date (UBD) printed on the label. |
| Initiation date | Jan 20, 2023 |
| Report date | Oct 25, 2023 |
| City | Minneapolis |
| State | MN |
| Country | United States |
| FEI number | 2182207 |
At a glance
- 1–9 Products in this recall
- 10–99 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: