PlainRecalls
FDA Devices Low Class III Ongoing

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

Reported: April 20, 2022 Initiated: January 24, 2022 #Z-0901-2022

Product Description

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

Reason for Recall

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.

Details

Recalling Firm
Volcano Corp
Units Affected
47
Distribution
US: CO, GA, MA, TX, AZ, NY, PA, CA, FL, MO, OR, MD, NC, TN OUS: JP, DE, GB, NL, IT
Location
San Diego, CA

Frequently Asked Questions

What product was recalled?
IntraSight Mobile IVUS Systems, Model: 797415, Part numbers: 300002018101, 300002018102. Recalled by Volcano Corp. Units affected: 47.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 20, 2022. Severity: Low. Recall number: Z-0901-2022.