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 / number Barcodes Product 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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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