Reported Apr 30, 2025 · Ongoing
Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
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 Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
- Lot codes and dates
Model No. 728242728243728244
- UDI
1,211 of 1,211 codes
(01)00884838098725(21)7014(01)00884838098725(21)7032(01)00884838059450(21)7056(01)00884838098725(21)7060(01)00884838098725(21)7062(01)00884838098725(21)7064(01)00884838098725(21)7072(01)00884838098725(21)7087(01)00884838059450(21)7096(01)00884838059450(21)7123(01)00884838059450(21)7124(01)00884838098725(21)7128(01)00884838098725(21)7135(01)00884838098725(21)7154(01)00884838098725(21)7163(01)00884838098725(21)7179(01)00884838098725(21)7191(01)00884838098725(21)7220(01)00884838098725(21)7221(01)00884838098725(21)7229(01)00884838059450(21)7240(01)00884838098725(21)7245(01)00884838098725(21)7246(01)00884838098725(21)7247(01)00884838098725(21)7254(01)00884838098725(21)7256(01)00884838098725(21)7282(01)00884838098725(21)7283(01)00884838098725(21)7292(01)00884838098725(21)7297(01)00884838098725(21)7304(01)00884838098725(21)7306(01)00884838098725(21)7309(01)00884838098725(21)7311(01)00884838098725(21)7331(01)00884838098725(21)7332(01)00884838059450(21)7333(01)00845225003036(10)0302624730(21)7336(01)00845225003036(10)0302624730(21)7341(01)00845225003036(10)0302624730(21)7345(01)00845225003036(10)0302624730(21)7348(01)00845225003036(10)0302624730(21)7353(01)00884838059450(21)7355(01)00884838059450(21)7362(01)00845225003036(10)0302624730(21)7364(01)00845225003036(10)0302624730(21)7367(01)00845225003036(10)0302624730(21)7373(01)00884838098725(21)7396(01)00845225003036(10)0302624730(21)7401(01)00845225003036(10)0302624730(21)7406(01)00884838098725(21)7410(01)00845225003036(10)0302624730(21)7414(01)00845225003036(10)0302624730(21)7421(01)00884838098725(21)7429(01)00884838098725(21)7441(01)00845225003036(10)0302624730(21)7442(01)00845225003036(10)0302624730(21)7443(01)00884838059450(21)7449(01)00845225003036(10)0302624730(21)7455(01)00845225003036(10)0302624730(21)7464
- Amount recalled
- 630 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Unintended motion issues related to Interventional Control that may lead to collision of the Gantry/table with the operator or patient.
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.
Free recall alerts
Get alerted about new Philips North America LLC recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.