Reported Oct 1, 2025 · Ongoing
Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.
Philips North America LLC
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 North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289
Is this the product you have?
- Philips
- CT systems labeled as the following1. Brilliance iCT
- Model Number728306
- Lot codes and dates
- 1
- Model Number728306
- UDI-DI00884838059474
- Serial Number
210 of 210 codes
10006810018810024110028810033210036510046185007850161006571006821006861007791008321007831007751007881008071008281008168513685153100043100038100082100074100081100097100098100119100111100113100123100130100133100222100141100134100160100157100150100158100180100161100173100215100064100117100247100172100196200045100191100374100189100230100203100201100204100211
- Amount recalled
- 210 units
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
- Nationwide
Why it was recalled
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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