FDA Device recall Z-1675-2013
AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892
- FDA Device
- Class II
- terminated
- Published 2013-07-17
On 2013-07-17 the FDA classified a Class II recall of AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892 by Angiodynamics, citing the RITA Main Cable product contains the incorrect Instructions for Use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1675-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-06-11 |
| Published | 2013-07-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Angiodynamics |
| Distribution | n/a |
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.
Reason
The RITA Main Cable product contains the incorrect Instructions for Use.
Identifiers
| code_info | Catalog #700-101892, Lot number: 30.12 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1675-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.