FDA Recall Terminated

RenovoCath RC 120; Temporary Intravascular Occluding Catheter Model number: MMRC120-DB-1111; Rx only. Cardiovascular: The RenovoCath RC120 Catheter is intended for the isolation of blood flow and delivery of fluids, including diagnostic and/or therapeutic agents, to selected sites in the peripheral vascular system.

Recall: Z-0565-2016 · Initiated November 25, 2015

Recall

Recall Number
Z-0565-2016
Event Number
72810
Firm
RenovoRx, Inc.
FEI Number
3011279674
Product Code
MJN
Status
Terminated
Root Cause
Labeling Change Control
Initiated
November 25, 2015
Posted
December 31, 2015
Terminated
February 29, 2016
Address
4546 El Camino Real, Ste 282, Los Altos, CA, 94022-1068

Description

RenovoCath RC 120; Temporary Intravascular Occluding Catheter Model number: MMRC120-DB-1111; Rx only. Cardiovascular: The RenovoCath RC120 Catheter is intended for the isolation of blood flow and delivery of fluids, including diagnostic and/or therapeutic agents, to selected sites in the peripheral vascular system.

Reason

Incorrect version of Instructions for Use were shipped to two US customers.

Action

RenovoRx notified customers by phone and by mail of this issue. This notification requests that the customers remove the affected product from their inventory and remove and replace the incorrect Instructions for Use with the correct Instructions for Use provided by RenovoRx. The customers are requested to return the incorrect Instruction for Use to RenovoRx for disposition and are requested to complete a Recall Confirmation Form enclosed to document the completion of the requested Correction. For further questions, please call (650) 284-4433.

Distribution

US Distribution to the states of : CA and FL.

Quantity

11 units