FDA Recall: Software system mixing patient records

Company: Volcano Corp
Date of Enforcement Report: 9/25/2026
Class: II

PRODUCT

Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA

Recall Number:

Z-3276-2026

REASON:

Software system may associate image data from one patient with another patient’s record, potentially resulting in incorrect diagnosis or treatment.

RECALLING FIRM/MANUFACTURER:

Volcano Corp

VOLUME:

19 systems

DISTRIBUTION:

Worldwide – US Nationwide distribution in the states of MA, MN, TX, AL, GA, CA and the countries of Belgium, Denmark, Germany, Netherlands, Poland, Spain, Sweden, United Kingdom.

About the author

Allison joined SoftwareCPR in 2022, bringing along over ten years of passion for building teamwork and growth in organizations. This is established in part by the greatest University the South has to offer- Mississippi State.

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Corporate Office

15148 Springview St.
Tampa, FL 33624
USA
+1-781-721-2921
Partners located in the US (CA, FL, MA, MN, TX) and Canada.