FDA Recall Open, Classified

IntraSight Mobile IVUS Systems, Model: 797415, Part numbers: 300002018101, 300002018102

Recall: Z-0901-2022 · Initiated January 24, 2022

Recall

Recall Number
Z-0901-2022
Event Number
89677
Firm
Volcano Corp
FEI Number
3008363989
Product Code
IYO
Status
Open, Classified
Root Cause
Error in labeling
Initiated
January 24, 2022
Address
3721 Valley Centre Dr, Ste 500, San Diego, CA, 92130-3328

Description

IntraSight Mobile IVUS Systems, Model: 797415, Part numbers: 300002018101, 300002018102

Reason

Multi-Modality Touch Screen Modules (MM-TSM), which are bedside/secondary control units, used as part of Mobile IVUS systems, are missing the following labeling information: Unique Device Identifier, Legal Manufacturer Information, Part Number, Rx Symbol, and Model Reference Information.

Action

On 01/24/22, correction notices were sent to customers who were informed that the recalling firm will notify all affected customers and arrange for a Field Service Engineer (FSE) to replace the MM-TSM free of charge. In addition, customers were asked to do the following: 1) Distributors or customers who have forwarded affected devices to other end users were asked to, send a copy of the correction notification to any customer to whom they have distributed affected devices to. 2) Customers were asked to complete and return customer response forms. 3) Customers with additional questions were encouraged to contact their local firm representative or contact IGTD Customer Service: Phone: 1-800-228-4728, Option 2, Email: [email protected], Hours of Operation: Monday - Friday 8:00AM - 5:00PM PST

Distribution

US: CO, GA, MA, TX, AZ, NY, PA, CA, FL, MO, OR, MD, NC, TN OUS: JP, DE, GB, NL, IT

Quantity

47