Philips recalls ProxiDiagnost N90 1.0 and 1.1 models with potential tabletop cable cracks that could prevent table tilting or braking. Affected units have specific serial numbers; stop use if table movement fails.
Potential table stop due to a broken tabletop cable: On the ProxiDiagnost N90 table there is a cable located under the tabletop that is covered by a plastic sleeve which can crack and damage the cable. If the tabletop cable breaks, the user may not be able to initiate table tilting movements or braking
Philips is recalling two versions of its ProxiDiagnost N90 medical imaging tables due to a risk that the tabletop cable could crack, causing the table to malfunction during tilting or braking. This could prevent the table from moving safely, potentially leading to injury if the table fails during use.
The tabletop cable is covered by a plastic sleeve that can crack, damaging the cable. If the cable breaks, the table may not tilt or brake properly, which could cause the table to become unstable during medical procedures.
Medical facilities using the ProxiDiagnost N90 1.0 (Model 706100) or 1.1 (Model 706110) tables are most at risk. Patients and staff could be affected if the table malfunctions during procedures.
Check for the ProxiDiagnost N90 1.0 (Model 706100) or 1.1 (Model 706110) models with serial numbers listed in the recall notice. The affected units have specific serial numbers starting with 10000000 through 10001116.
Test if the table can tilt or brake as usual; if it fails, stop using it immediately.
ProxiDiagnost N90 1.0 (Model 706100) and 1.1 (Model 706110) with specific serial numbers listed in the recall notice.
Check if your table has serial numbers starting with 10000000 through 10001116 as listed in the recall notice.
Stop using the table immediately and contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1477-2023 — Philips Philips Hello, I own a Philips that is covered by recall Z-1477-2023 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.
