Drug recall
Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip Model Number: C-1010-R-18…
FDA recall event 73407 · Class II · Neurotherm, Inc.
Key facts
| Event ID | 73407 |
|---|---|
| Recall numbers | Z-1247-2016 |
| Recalling firm | Neurotherm, Inc. |
| Product type | Devices |
| Products | Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip Model Number: C-1010-R-18 Product Usage: The device is a radiofrequency needle, used for the application of… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Straight needle labeled as a curved needle |
| Initiation date | Feb 26, 2013 |
| Report date | Mar 30, 2016 |
| Termination date | Mar 25, 2016 |
| City | Wilmington |
| State | MA |
| Country | United States |
| FEI number | 3002953813 |
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: