Philips recalls ProxiDiagnost R90 1.0 and 1.1 models (706100/706110) due to risk of electrical fire from power surges causing short circuits in the main 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 ProxiDiagnost R90 1.0 and 1.1 multi-functional systems because power surges can cause short circuits in the main cabinet, potentially leading to electrical fires. This affects units with specific model numbers and serial ranges.
If the system encounters an overvoltage or power surge, it can create a short circuit inside the main cabinet. This may lead to electrical fires, smoke, or popping sounds from the cabinet.
Users of the Philips ProxiDiagnost R90 1.0 and 1.1 systems with model numbers 706100 or 706110 are most at risk if they experience power surges, as the system may overheat and cause a fire.
Check for model numbers 706100 or 706110 on the device. Serial numbers start with 597241 or 10000000 through 10001116. The product was sold in the U.S. between 2020 and 2023.
If you hear popping sounds or smell smoke from the cabinet, stop using the device immediately.
Reach out to Philips customer service for assistance with the recall process.
Model numbers 706100 and 706110.
Check for model numbers 706100 or 706110 and serial numbers starting with 597241 or 10000000 through 10001116.
The recall record does not specify a remedy.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1356-2023 — Philips Philips Hello, I own a Philips that is covered by recall Z-1356-2023 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.
