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
February 7, 2024FDAAchieva 1.5T Initial system. Model (REF) Numbers 781178.Z-0947-2024
February 7, 2024FDASmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270, 782113, 782129.Z-0956-2024
February 7, 2024FDAAchieva XR. Model (REF) Numbers 781153, 781253.Z-0949-2024
January 31, 2024FDASmartPath to dStream for 1.5T, Model No. 781260, 782112Z-0812-2024
January 31, 2024FDAAchieva 1.5T, Model No. 781178, 781196, 781296Z-0807-2024
January 31, 2024FDAAchieva 3.0T, Model No. 781177Z-0809-2024
January 31, 2024FDAIntera 1.5T, Model No. 781195Z-0811-2024
January 31, 2024FDAIngenia Ambition X, Model No. 782109Z-0810-2024
January 31, 2024FDAAchieva 1.5T Conversion, Model No. 781283Z-0808-2024
January 24, 2024FDA(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Ex…Z-0731-2024
January 24, 2024FDA(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436Z-0732-2024
January 24, 2024FDAIncisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cab…Z-0719-2024
January 17, 2024FDA(1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product Number 7…Z-0715-2024
January 17, 2024FDABrightView X, Gamma Camera, Product Code 882478Z-0678-2024
January 17, 2024FDABrightView, Gamma Camera System, Product Code 882480.Z-0677-2024
January 17, 2024FDABrightView XCT, Gamma Camera, Product Code 882482Z-0679-2024

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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