Reported Sep 30, 2026 · Ongoing · Updated Oct 6, 2026
MR 5300 Model Number (REF): 1. 782110, 2. 782152;
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?
- MR 5300 Model Number (REF)
1. 7821102. 782152
- Lot codes and dates
- 1
- Model Number (REF)782110
- UDI-DI884838099364
- Serial Numbers
447 of 447 codes
633836338463385633866342263435636436334663021630546309163092631136331363314633156332263521635246356563572635936360463639636946369763705637066370763716637216372763736637376373963743637506375363754637556376963773636176356063038634846302363064630666307563086631496316163183631946319563198631996330863319
- Model Number (REF)782152
- UDI-DIN/A
- Serial Numbers
165 of 165 codes
693046934969098691016925069318693216933869238692396902469026690346903969046690816908369105691516923569023690376904169066691126915269233693026929969193691946924169287693206907069071691066911069127691616936069366690446904569048691166928669300693516905569073690756908669191692076924369252692586926069261
- Amount recalled
- 611
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
- Nationwide
- GA
Why it was recalled
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.
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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