Hazard

Alignment Error recalls

17 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 17
Critical: 0
Severe: 0
Most recent: 2025-05-28

Of the 17 alignment error recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all alignment error recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–17 of 17

HighFDA (Devices)·Z-1791-2025·2025-05-28
SmartPath to Ingenia Elition X MRI Systems Alignment Error Recall
Philips is recalling SmartPath to Ingenia Elition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. The alignment errors could affect image interpretation.
Product
Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1801-2025·2025-05-28
Philips Ingenia Ambition X MRI Systems Alignment Error in MobiView
Philips is recalling certain Ingenia Ambition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1805-2025·2025-05-28
Philips MR 7700 Medical Device Alignment Error in MobiView Application
Philips is recalling MR 7700 model medical devices due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1789-2025·2025-05-28
SmartPath to dStream 3.0T Medical Device Recall for Software Error
Philips is recalling the SmartPath to dStream 3.0T medical device due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. This could affect image interpretation accuracy.
Product
Product Name: SmartPath to dStream for 3.0T; Model Number: 782145
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1790-2025·2025-05-28
Philips SmartPath to dStream Medical Imaging Software Alignment Error
Philips is recalling SmartPath to dStream for XR and 3.0T medical imaging software due to potential alignment errors in cross reference line functionality when reviewing images with the MobiView application.
Product
Product Name: SmartPath to dStream for XR and 3.0T; Model Numbers: (1) 781270, (2) 782113;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1798-2025·2025-05-28
Ingenia Ambition S MRI devices recalled for alignment errors
Philips is recalling certain Ingenia Ambition S MRI devices due to potential alignment errors in the cross reference line functionality when reviewing images with the MobiView application.
Product
Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1804-2025·2025-05-28
MR 5300 Medical Device Recall for Cross Reference Line Alignment Error
Philips is recalling MR 5300 medical devices (Model Numbers 782110 and 782152) due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1803-2025·2025-05-28
Philips Ingenia Elition X MRI System Alignment Error Recall
Philips has recalled specific Ingenia Elition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1802-2025·2025-05-28
Philips Ingenia Elition S MRI System Alignment Error Recall
Philips is recalling certain Ingenia Elition S MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1796-2025·2025-05-28
Philips Ingenia 1.5T S MRI System Alignment Error Recall
Philips is recalling the Ingenia 1.5T S magnetic resonance imaging (MRI) system due to potential alignment errors in cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia 1.5T S; Model Number: 781347;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1800-2025·2025-05-28
Ingenia 3.0T CX MRI System Alignment Error in Cross Reference Line
Philips is recalling the Ingenia 3.0T CX MRI system due to potential alignment errors in the cross reference line when using the MobiView application to review images. The alignment error could affect image accuracy during review.
Product
Product Name: Ingenia 3.0T CX; Model Number: 781271;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1795-2025·2025-05-28
Ingenia 1.5T MRI Systems Recalled for Alignment Errors
Philips is recalling Ingenia 1.5T MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images with the MobiView application.
Product
Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1788-2025·2025-05-28
Philips SmartPath to dStream 1.5T medical device alignment recall
Philips is recalling certain SmartPath to dStream 1.5T medical imaging devices due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1794-2025·2025-05-28
Philips Evolution Upgrade 3.0T MRI Cross Reference Line Alignment Error
Philips is recalling Evolution Upgrade 3.0T MRI systems (Models 782117 and 782143) due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1793-2025·2025-05-28
Evolution Upgrade 1.5T imaging system alignment error recall
Philips Evolution Upgrade 1.5T medical imaging systems may display alignment errors in cross-reference line functionality when reviewing images via MobiView application.
Product
Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1792-2025·2025-05-28
Philips Upgrade to MR 7700 Medical Device Alignment Error Recall
Philips is recalling the Upgrade to MR 7700 (Model 782130) due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. The misalignment could affect diagnostic accuracy.
Product
Product Name: Upgrade to MR 7700; Model Number: 782130;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1797-2025·2025-05-28
Ingenia 3.0T MRI Systems Recalled for Image Alignment Errors
Philips is recalling certain Ingenia 3.0T MRI systems worldwide due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;
Category
Medical Device
Distribution
Distributed nationwide