Lower riskMedical device recall · FDA · Published May 2, 2024
Philips Interventional Hemodynamic Software Recall: Potential Pressure Wave Data Sync
Philips recalls certain versions of Interventional Hemodynamic Application software (R.1.2X, R.1.3.0, R1.2.1) due to potential pressure wave data synchronization errors between devices.
“Philips Interventional Hemodynamic Software Recall: Potential Pressure Wave Data Sync.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/55284-philips-interventional-hemodynamic-software-recall-potential-pressure-wave-data-sync. Based on FDA recall #Z-1926-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1926-2024%22&limit=1).
The FDA announced on May 2, 2024, that Philips Medical Systems Nederland B.V. is recalling its Interventional Hemodynamic Application software due to potential pressure wave data synchronization errors between devices. The agency issued recall number Z-1926-2024 for the Class II device.
The software enables invasive investigation of cardiac and vascular diseases. The recall cites a potential for pressure wave data synchronization from two devices to be incorrect.
Context
GovInfoNow's records show Philips Medical Systems Nederland B.V. has issued 58 other recalls since May 26, 2021. Recent brand actions include recalls on July 16, 2026, involving potential image quality degradation and loss of geometry movements in Azurion R2.2.10 Systems. Other recent recalls of similar products include Philips Cardiac Workstation 5000 (July 1, 2026), Philips Cardiac Workstation 7000 (July 1, 2026), and Philips PIC iX Essentials Software Freezes (July 31, 2026).
How to tell if you have this one
Check if your software version is R.1.2X, R.1.3.0, or R1.2.1. The model number is 722467. Serial numbers include CZC9509HWC, CZC950919K, CZC9509HTZ, and others listed in the recall notice.
Brand
Philips
Product
Philips Interventional Hemodynamic Application R.1.2X, R.1.3.0, R1.2.1. Software that enables invasive investigation of
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Software Version
Verify your software version by checking the device settings or documentation. The affected versions are R.1.2X, R.1.3.0, and R1.2.1.
Contact Philips Support
Reach out to Philips customer support for assistance with the recall and to determine if your device is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 3 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide distribution - US Nationwide in the states of CA, IN, OR and the countries of Argentina, Australia, Austria, Bangladesh, Belgium, Bulgaria, Chile, Costa Rica, C¿te D'Ivoire, Czech Republic, Ecuador, France, Germany, Gibraltar,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Indiana, Oregon.
Recall timeline
FDA published this recall 34 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 recall indicates a potential for incorrect pressure wave data synchronization between devices, which could lead to inaccurate measurements during procedures. However, the hazard is not described as causing serious injury or death.
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-1926-2024 (May 2, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1926-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.