Class II — Angiodynamics, INC
| Recalling firm | AngioDynamics |
|---|---|
| Registered facility | EXIMO MEDICAL LTD (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The RITA Main Cable product contains the incorrect Instructions for Use. |
| Product | 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. |
| Quantity | 13 units |
| Distribution | Worldwide Distribution, including the US, Austria, China, Italy, Russia and the UK. |
| Initiated | 2013-06-11 |
| Classified | 2013-07-10 |
| Terminated | 2015-06-12 |
| Recall number | Z-1675-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Angiodynamics, INC (Z-1675-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65439/
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