Philips recalls CombiDiagnost R90 model 709031 produced July 2024-June 2025 due to potential difficulty moving ceiling suspension telescopic carriages requiring extra force. Affected units may need special handling.
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
Philips is recalling CombiDiagnost R90 devices with model number 709031 made between July 2024 and June 2025 because some ceiling suspension telescopic carriages may require extra force to move vertically. This could make the device harder to adjust safely during use.
The ceiling suspension telescopic carriage in some units may require additional physical effort to move vertically. This could lead to increased strain during device adjustments, though serious injury is not expected.
Users of Philips CombiDiagnost R90 devices with model number 709031 produced from July 2024 through June 2025 are affected. Medical professionals using these devices for diagnostic purposes may be most at risk due to potential handling challenges.
Check for model number 709031 on your CombiDiagnost R90 device. Units produced between July 2024 and June 2025 are affected. The serial numbers listed in the recall notice include 100001385 through 100001488.
Verify your CombiDiagnost R90 has model number 709031.
Reach out to Philips Medical Systems for specific guidance on handling the device.
Philips identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may require additional force to move vertically due to potential manufacturing issues.
No, the recall does not require stopping use. The device can be used with caution after verifying the model number and contacting Philips for guidance.
Check your model number and contact Philips Medical Systems for specific handling instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0462-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0462-2026 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.
