Philips recalls CombiDiagnost R90 1.0 and 1.1 multi-functional systems (model 709030/709031) due to overvoltage causing electrical fire risk. Affected units may show smoke, popping sounds, or fire in the cabinet.
If the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical fire within the cabinet, see or smell smoke emitting from the cabinet, or hear a popping sound coming from the cabinet.
Philips is recalling CombiDiagnost R90 1.0 and 1.1 multi-functional systems (model numbers 709030 and 709031) because electrical overvoltage can cause short circuits and fire in the cabinet. This poses a risk of fire, smoke, or popping sounds if the system experiences a power surge.
If the system experiences an overvoltage or power surge, it can cause a short circuit inside the main cabinet. This may lead to electrical fire, smoke emission, or popping sounds from the cabinet.
Users of the CombiDiagnost R90 1.0 and 1.1 systems with model numbers 709030 or 709031 are affected. Those who have the system installed in a home or business setting are most at risk if power surges occur.
Check for model numbers 709030 or 709031 on the product label. The system may also have serial numbers starting with 10000000 through 10000199 or higher as listed in the recall notice.
Look for smoke, popping sounds, or a burning smell from the cabinet to determine if the system is already affected.
Immediately stop using the system if you notice smoke, popping sounds, or a burning smell from the cabinet.
Model numbers 709030 and 709031 for CombiDiagnost R90 1.0 and 1.1 systems.
Check the model number on the product label; affected units have model numbers 709030 or 709031.
The recall record does not specify a remedy, so no fix is provided.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1355-2023 — Philips Philips Hello, I own a Philips that is covered by recall Z-1355-2023 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.
