Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1675-2013 — 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.

U.S. FDA — Device Enforcement · United States · 2013-06-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1675-2013
Date of alert
2013-06-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Angiodynamics, INC
Product category
device
Product type
Devices
Reported risk: The RITA Main Cable product contains the incorrect Instructions for Use.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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