Drug recall
AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables are indicated for use with…
FDA recall event 65439 · Class II · Angiodynamics, INC
Key facts
| Event ID | 65439 |
|---|---|
| Recall numbers | Z-1675-2013 |
| Recalling firm | Angiodynamics, INC |
| Product type | Devices |
| Products | AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables are indicated for use with the RITA RF Generators and RITA electrosurgical devices. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The RITA Main Cable product contains the incorrect Instructions for Use. |
| Initiation date | Jun 11, 2013 |
| Report date | Jul 17, 2013 |
| Termination date | Jun 12, 2015 |
| City | Manchester |
| State | GA |
| Country | United States |
| FEI number | 1000111164 |
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: