Philips North America Llc: 179 recalls on record

Recalls filed with 1 agency: FDA (179).

First recall on record: April 5, 2017. Most recent: September 9, 2026.

Risk classification: Class I: 5 · Class II: 174

Most recent recalls

DateAgencyProduct
February 12, 2025FDAIntelliVue Patient Monitor MX550. Model Number: 866066Z-1110-2025
December 25, 2024FDAPhilips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216Z-0686-2025
December 11, 2024FDASpectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.Z-0583-2025
December 4, 2024FDAdS Breast 7ch 3.0TZ-0540-2025
December 4, 2024FDAMammotrak Diagnostic Coil 1.5TZ-0541-2025
December 4, 2024FDAMammotrak Diagnostic Coil 3.0TZ-0543-2025
December 4, 2024FDAST SENSE Breast CoilZ-0547-2025
December 4, 2024FDAAchieva TX Interventional Coil 3.0TZ-0536-2025
December 4, 2024FDAdS Breast 16ch 3.0TZ-0538-2025
December 4, 2024FDAST SENSE Breast Dx CoilZ-0548-2025
December 4, 2024FDAMammotrak Interventional Coil 1.5TZ-0542-2025
December 4, 2024FDASENSE Breast CoilZ-0545-2025
December 4, 2024FDAdS Breast 7ch 1.5TZ-0539-2025
December 4, 2024FDAMammotrak Interventional Coil 3.0TZ-0544-2025
December 4, 2024FDASENSE Breast Coil 3.0T 7chZ-0546-2025
December 4, 2024FDAdS Breast 16ch 1.5TZ-0537-2025
October 16, 2024FDAIntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and orde…Z-0020-2025
October 9, 2024FDADIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system central …Z-3312-2024
October 2, 2024FDASmartPath to dStream for XR and 3.0T- For use as a diagnostic device to obtain cross-sec…Z-3204-2024
October 2, 2024FDAEvolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectional images,…Z-3193-2024
October 2, 2024FDAIngenia Elition S -For use as a diagnostic device to obtain cross-sectional images, spect…Z-3199-2024
October 2, 2024FDAIngenia Ambition X - For use as a diagnostic device to obtain cross-sectional images, spe…Z-3198-2024
October 2, 2024FDAIngenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectr…Z-3196-2024
October 2, 2024FDAIngenia 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectrosc…Z-3195-2024
October 2, 2024FDASmartPath to dStream for 1.5T - For use as a diagnostic device to obtain cross-sectional …Z-3203-2024

Questions about this company

How many recalls does Philips North America Llc have?
Recalert has 179 U.S. recalls on record for Philips North America Llc, published between April 5, 2017 and September 9, 2026.
Which agencies have handled Philips North America Llc recalls?
Philips North America Llc appears as the recalling firm in recalls from: FDA (179).

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