Lower riskMedical device recall · FDA · Published April 7, 2025
Philips IntelliSpace Cardiovascular Software Recalls: Missing Report Data Risk
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.
“Philips IntelliSpace Cardiovascular Software Recalls: Missing Report Data Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52484-philips-intellispace-cardiovascular-software-recalls-missing-report-data-risk. Based on FDA recall #Z-1740-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1740-2025%22&limit=1).
The FDA announced on April 7, 2025, that Philips Medical Systems Nederland B.V. is recalling IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x due to a hazard involving missing or incomplete information in reports when using the Echo Module. The agency issued recall number Z-1740-2025 for the voluntary Class II action affecting 996 units.
How to tell if you have it
Brand: Philips
Product: IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x
Model Number: 830089
UPC: 00884838106970
UPC: 00884838115378
UPC: 00884838122000
The hazard
According to the FDA, an issue was identified with the software when using the Echo Module of ISCV. The hazard may result in missing or incomplete information in the report.
Context
GovInfoNow's records show Philips Medical Systems Nederland B.V. has had 58 other recalls on record since May 26, 2021. Recent similar recalls include a July 31, 2026 recall for Philips PIC iX Essentials Software Freezes and a July 1, 2026 recall for the Philips Cardiac Workstation 7000 involving inaccurate heart rate data risk.
How to tell if you have this one
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.
Brand
Philips
Product
IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x; Model Number: 830089
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Software Version
Identify your software version by checking the version number on the device or software interface.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Domestic: Nationwide Distribution International: Australia, Austria, Belgium, Canada, Denmark, Estonia, Finland, France, Germany, Greece, Hong Kong, Indonesia, Ireland, Italy, Japan, Luxembourg, Mexico, Netherlands, Norway, Poland, Saudi…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 37 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-1740-2025 (April 7, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1740-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.