Philips recalls DigitalDiagnost C90 Flex/Value/Chest/ER models 712035 without seismic kit for wall stands, risking instability during earthquakes.
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
Philips is recalling DigitalDiagnost C90 Flex/Value/Chest/ER models 712035 that were shipped without the required seismic kit for wall stands. This could lead to instability during earthquakes, potentially causing damage or injury.
The wall stand may become unstable during earthquakes without the required seismic kit, which is designed to prevent damage and ensure stability. This could lead to the device falling or causing injury.
Owners of DigitalDiagnost C90 Flex/Value/Chest/ER models 712035 sold in the U.S. are affected. Those using the wall stand without the seismic kit are at higher risk during seismic events.
Check for model number 712035 on the device. The product was sold in the U.S. with lot code 24861049.
Ensure the wall stand has the seismic kit installed before use during earthquakes.
The wall stand was delivered without the required seismic kit, which is designed to prevent damage and ensure stability during earthquakes.
Model number 712035.
The official recall does not specify a fix; the product was shipped without the seismic kit.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2354-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-2354-2026 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.
