Reported Nov 19, 2025 · Ongoing

ProxiDiagnost N90; Model Number: 706110;

Philips Medical Systems DMC GmbH

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips Medical Systems DMC GmbH · Development And Manufacturing Ctr. · Hamburg · N/A

Is this the product you have?

  • ProxiDiagnost N90
  • Model Number706110
Lot codes and dates

3 of 3 products

Products covered by this recall
Model / numberBarcodesProduct as published
706110
00884838103221UDI-DI: 00884838103221
Serial Number: 10001185, 10001205, 10001220, 10001224, 10001225, 10001227, 10001228, 10001229, 10001230, 10001231, 10001234, 10001235, 10001236, 10001237, 10001239, 10001245, 10001247, 10001248, 10001249, 10001250, 10001251, 10001253, 10001256, 10001257, 10001258, 10001261, 10001262, 10001264, 10001265, 10001266, 10001269, 10001270, 10001271, 10001272, 10001273, 10001274, 10001275, 10001276, 10001277, 10001278, 10001282
Amount recalled
41 units

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide

Why it was recalled

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.