AngioDynamics RITA Main Cable — Class II medical device recall Z-1675-2013
Terminated recall by Angiodynamics, INC, reported 2013-07-17. The RITA Main Cable product contains the incorrect Instructions for Use.
| Recall number | Z-1675-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics, INC, Manchester, GA, United States |
| Recall initiated | 2013-06-11 |
| Classified | 2013-07-10 |
| Reported by FDA | 2013-07-17 |
| Terminated | 2015-06-12 |
| Countries outside the US | AT, CN, GB, IT, RU |
| Quantity | 13 units |
| Lot numbers | 30.12 |
| Model numbers | 700-101892 |
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 for recall
The RITA Main Cable product contains the incorrect Instructions for Use.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1675-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.