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.
Potential for pressure wave data synchronization from two devices may not be correct.
Philips is recalling specific versions of its Interventional Hemodynamic Application software that may cause incorrect pressure wave data synchronization between devices. This could lead to inaccurate medical measurements during cardiac and vascular procedures.
The software may not synchronize pressure wave data correctly between two devices. This could result in inaccurate measurements during invasive cardiac and vascular procedures, potentially affecting treatment decisions.
Healthcare professionals using Philips Interventional Hemodynamic Application software versions R.1.2X, R.1.3.0, R1.2.1 are most at risk. The recall affects medical devices used in cardiac and vascular procedures.
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.
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.
Reach out to Philips customer support for assistance with the recall and to determine if your device is affected.
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.
Check your software version and contact Philips customer support to determine if your device is affected. They will provide guidance on next steps.
The affected software versions are R.1.2X, R.1.3.0, and R1.2.1. The model number is 722467, and serial numbers include CZC9509HWC, CZC950919K, CZC9509HTZ, and others listed in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1926-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1926-2024 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.
