Philips recalls EasyDiagnost Eleva DRF X-ray systems with model 706050 due to potentially incorrect thermo switches in the power supply causing system malfunctions. Affected units have specific serial numbers listed in the recall notice.
Thermo switches in the main power supply for the system may be incorrectly installed, resulting in a malfunction.
Philips is recalling certain EasyDiagnost Eleva DRF X-ray systems (model 706050) because thermo switches in the power supply might be installed incorrectly, which could lead to system malfunctions. This recall affects medical facilities that use these X-ray systems for diagnostics.
The thermo switches in the main power supply may be incorrectly installed, causing the X-ray system to malfunction. This could potentially lead to improper operation of the system during diagnostic procedures, but the recall does not indicate a risk of injury or damage to users.
Medical facilities that own or use the recalled EasyDiagnost Eleva DRF X-ray systems (model 706050) are most at risk. The recall does not apply to individual consumers.
Check if your EasyDiagnost Eleva DRF X-ray system has model number 706050 and the specific serial numbers listed in the recall notice. The product is used for general-purpose diagnostic X-ray imaging in medical settings.
Check the model number on your EasyDiagnost Eleva DRF X-ray system; it should be 706050 if it is affected.
Reach out to Philips customer support to confirm if your specific serial number is listed in the recall and to get instructions for next steps.
The recall indicates a potential malfunction risk due to incorrect thermo switch installation, but the product is not unsafe for use in normal conditions. Affected units should be checked for the specific model and serial numbers listed.
Check if your EasyDiagnost Eleva DRF X-ray system has model number 706050 and a serial number from the list provided in the recall notice.
Contact Philips customer support to determine if your specific serial number is affected and to receive instructions for next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2523-2020 — Philips Philips Hello, I own a Philips that is covered by recall Z-2523-2020 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.
