Philips North America: 66 recalls on record

Recalls filed with 1 agency: FDA (66).

First recall on record: January 17, 2024. Most recent: September 23, 2026.

Risk classification: Class I: 3 · Class II: 57 · Class III: 6

Most recent recalls

DateAgencyProduct
August 6, 2025FDAIngenia 1.5T S Model Number (REF): 781347;Z-2205-2025
August 6, 2025FDAIngenia 3.0T Model Numbers (REF): (1) 781342, (2) 781377, (3) 782103;Z-2206-2025
October 16, 2024FDAPatient Information Center iX, Product Code 866386, and Patient Information Center iX Exp…Z-0035-2025
October 9, 2024FDAIntelliVue G7m Anesthesia Gas Module, Product Number 866173Z-0007-2025
October 2, 2024FDAIntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX45…Z-3249-2024
April 17, 2024FDAPHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5…Z-1507-2024
April 3, 2024FDAPatient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and…Z-1386-2024
April 3, 2024FDACareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), S…Z-1387-2024
February 21, 2024FDAProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) syste…Z-1073-2024
February 21, 2024FDAProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Re…Z-1072-2024
February 14, 2024FDABrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit forma…Z-0929-2024
February 14, 2024FDAIngenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 98971000873…Z-0975-2024
February 14, 2024FDAIngenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), pa…Z-0973-2024
February 14, 2024FDABrightView XCT, gamma camera for SPECT; Model Nos.: 6-digit format 882482; 12-digi…Z-0931-2024
February 14, 2024FDABrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit …Z-0930-2024
February 14, 2024FDAIngenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732…Z-0974-2024
February 7, 2024FDAIngenia 3.0T CX. Model (REF) Numbers 781271, 782105.Z-0951-2024
February 7, 2024FDAIntera Achieva 1.5T Pulsar. Model (REF) Number 781171.Z-0954-2024
February 7, 2024FDAIngenia 1.5T CX. Model (REF) Numbers 781262, 781261.Z-0950-2024
February 7, 2024FDASmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112.Z-0955-2024
February 7, 2024FDAAchieva 1.5T Conversion. Model (REF) Numbers 781346, 781283.Z-0946-2024
February 7, 2024FDAIntera 1.5T Achieva Nova-Dual. Model (REF) Number 781173.Z-0953-2024
February 7, 2024FDAAchieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.Z-0948-2024
February 7, 2024FDAAchieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.Z-0945-2024
February 7, 2024FDAIntera 1.5T Achieva Nova. Model (REF) Numbers 781172.Z-0952-2024

Questions about this company

How many recalls does Philips North America have?
Recalert has 66 U.S. recalls on record for Philips North America, published between January 17, 2024 and September 23, 2026.
Which agencies have handled Philips North America recalls?
Philips North America appears as the recalling firm in recalls from: FDA (66).

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