FDA Recall Terminated

Prestige Plus 185cm J-Tip: Part number: 9185J; Product Usage: The Prestige Plus Wire is indicated for use to measure pressure in blood vessels including both coronary and peripheral vessels, during diagnostic angiography and/or any interventional procedures. Blood pressure measurements provide hemodynamic information for the diagnosis and treatment of blood vessel disease.

Recall: Z-1845-2015 · Initiated June 4, 2015

Recall

Recall Number
Z-1845-2015
Event Number
71537
Firm
Volcano Corporation
FEI Number
2939520
Product Code
DQX
Status
Terminated
Root Cause
Labeling mix-ups
Initiated
June 4, 2015
Posted
June 25, 2015
Terminated
October 27, 2015
Address
2870 Kilgore Rd, Rancho Cordova, CA, 95670-6133

Description

Prestige Plus 185cm J-Tip: Part number: 9185J; Product Usage: The Prestige Plus Wire is indicated for use to measure pressure in blood vessels including both coronary and peripheral vessels, during diagnostic angiography and/or any interventional procedures. Blood pressure measurements provide hemodynamic information for the diagnosis and treatment of blood vessel disease.

Reason

During a relabeling procedure at the manufacturing facility, the products were labeled with a shelf life in accordance with the date of the relabeling and not in accordance with the original shelf life date at the time of manufacture

Action

Volcano sent an Urgent Medical Device Recalls lettersdated June 4, 2015 via Federal Express to affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to examine product inventory, quarantine the affected product, complete the attached Customer Return form, and contact Volcano Customer Service at 800-228-4728, option 4 to arrange for the return of any product in inventory.

Distribution

US Nationwide Distribution and one account in Canada.

Quantity

162 total (both devices)