Philips recalls specific software versions for IntelliSpace Cardiovascular systems due to potential missing or incomplete report data. Affected units may require updates to prevent inaccurate medical reports.
An issue was identified with the software when using the Echo Module of ISCV, the issue may result in missing or incomplete information in the report.
Philips is recalling certain versions of its IntelliSpace Cardiovascular software because they might cause reports to be missing or incomplete. This could lead to inaccurate medical information being sent to healthcare providers.
The software issue can cause reports to be missing or incomplete when using the Echo Module. This might result in inaccurate medical information being sent to healthcare providers, potentially affecting patient care decisions.
Healthcare providers using the affected software versions for cardiac imaging may be impacted. Medical staff handling reports generated by these versions are most at risk.
Check if your IntelliSpace Cardiovascular software is version 6.x, 7.x, or 8.x with model number 830089. The specific software versions listed in the recall include 6.1.0.0 through 8.0.0.0.
Identify your software version by checking the version number on the device or software interface.
Software versions 6.x, 7.x, and 8.x with model number 830089, including specific versions like 6.1.0.0 through 8.0.0.0.
Check if your IntelliSpace Cardiovascular software is version 6.x, 7.x, or 8.x with model number 830089 as listed in the recall.
The recall does not specify a remedy, so you should check with Philips for updates or guidance on potential fixes.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1740-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1740-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
