Reported Sep 30, 2026 · Ongoing · Updated Oct 6, 2026
Achieva 3.0T; Model Numbers (REF): 1. 781177, 2. 781277, 3. 781278, 4. 781344, 5. 781345;
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?
- Achieva 3.0T
- Model Numbers (REF)
1. 7811772. 7812773. 7812784. 7813445. 781345
- Lot codes and dates
5 of 5 products
Products covered by this recall # Product as published 1 Model Numbers (REF): 781177; UDI-DI: N/A; Serial Numbers: 17144, 17376, 17448, 24049, 17099, 24138, 24060, 17607, 17079, 17146, 17189, 17379, 17469, 17270, 17432, 17279, 17233, 17295, 17446, 17362, 24068, 24096, 17139, 24037, 24099, 17535, 24079, 17030, 17043, 17056, 17114, 17149, 17161, 17167, 17170, 17179, 17216, 17217, 17235, 17251, 17316, 17319, 17365, 17453, 17494, 17523, 17558, 17561, 24038, 24070, 24089 2 Model Numbers (REF): 781277; UDI-DI: N/A; Serial Numbers: 34289, 34213, 34276, 34113, 34123, 34239, 34264, 34274, 34285, 34095, 34138, 34305, 34118, 34106, 34159, 34241, 34263, 34139, 34002, 34029, 34034, 34071, 34201 3 Model Numbers (REF): 781278; UDI-DI: N/A; Serial Numbers: 38326, 38346, 38043, 38098, 38108, 38152, 38157, 38194, 38210, 38212, 38215, 38231, 38233, 38236, 38238, 38240, 38267, 38269, 38270, 38271, 38284, 38312, 38321, 38328, 38332, 38338, 38339, 38340, 38344, 38349, 38367, 38370, 38401, 38402, 38405, 38407, 38408, 38412, 38415, 38420, 38421, 38423, 38425, 38426, 38427, 38430, 38431, 38432, 38433, 38437, 38439, 38441, 38442, 38443, 38445, 38447, 38448, 38450, 38453, 38454, 38456, 38457, 38458, 38288, 38079, 38139, 38228, 38145, 38034, 38251, 38278, 38207, 38061, 38086, 38095, 38115, 38133, 38017, 38064, 38112, 38143, 38160, 38183, 38229, 38256, 38296, 38297, 38315, 38331, 38272, 38322, 38323, 38337, 38345, 38077, 38200, 38268, 38090, 38188, 38093, 38012, 38099, 38003, 38057, 38072, 38085, 38016, 38033, 38091, 38103, 38173, 38341, 38232 4 Model Numbers (REF): 781344; UDI-DI: N/A; Serial Numbers: 73005, 73008, 73009, 73006, 73010 5 Model Numbers (REF): 781345; UDI-DI: N/A; Serial Numbers: 74027, 74035, 74039, 74047, 74052, 74001, 74010, 74026, 74046, 74005, 74007, 74021, 74030, 74040, 74044, 74048, 74032, 74037 - Amount recalled
- 210
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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