Reported Nov 19, 2025 · Ongoing
CombiDiagnost R90; Model Number: 709031;
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?
- CombiDiagnost R90
- Model Number709031
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 709031— — 00884838101456UDI-DI: 00884838101456 — Serial Number: 100001385, 100001402, 100001409, 100001412, 100001415, 100001416, 100001417, 100001424, 100001426, 100001432, 100001449, 100001460, 100001464, 100001476, 100001480, 100001483, 100001488 - Amount recalled
- 17 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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