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
October 2, 2024FDAIngenia Ambition S - For use as a diagnostic device to obtain cross-sectional images, spe…Z-3197-2024
October 2, 2024FDAMR 7700 -For use as a diagnostic device to obtain cross-sectional images, spectroscopic …Z-3202-2024
October 2, 2024FDAIngenia Elition X- For use as a diagnostic device to obtain cross-sectional images, spect…Z-3200-2024
October 2, 2024FDAIngenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectrosco…Z-3194-2024
October 2, 2024FDASmartPath to Ingenia Elition X - For use as a diagnostic device to obtain cross-sectional…Z-3205-2024
October 2, 2024FDAMR 5300 - For use as a diagnostic device to obtain cross-sectional images, spectroscopic …Z-3201-2024
August 14, 2024FDAIntelliVue Patient Monitor MX550 with L.x and M.x; K.x provided with L.x entitlements Mo…Z-2511-2024
August 14, 2024FDAIntelliVue Patient Monitor MX400 with L.x and M.x; K.x provided with L.x entitlements Mo…Z-2508-2024
August 14, 2024FDAIntelliVue Patient Monitor MX500 with L.x and M.x; K.x provided with L.x entitlements Mo…Z-2510-2024
August 14, 2024FDAIntelliVue Patient Monitor MX450 with L.x and M.x; K.x provided with L.x entitlements M…Z-2509-2024
July 10, 2024FDAAvalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the fetal heart a…Z-2239-2024
July 3, 2024FDASENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil for torso and abdomen imaging …Z-2165-2024
July 3, 2024FDASENSE XL TORSO COIL 1.5T. 16-element receive only coil for torso and abdomen imaging in P…Z-2163-2024
July 3, 2024FDASENSE XL TORSO COIL 3.0T. 16-element receive only coil for torso and abdomen imaging in P…Z-2164-2024
June 12, 2024FDAHA FlexTrak II-Patient transport functionality to transport the patient from the preparat…Z-1950-2024
June 12, 2024FDAHA FlexTrak-Patient transport functionality to transport the patient from the preparation…Z-1948-2024
June 12, 2024FDAHA FlexTrak-Patient transport functionality to transport the patient from the preparation…Z-1949-2024
May 29, 2024FDAMR system 1.5T Marlin- Magnetic Resonance (MR) systems are Medical Electrical Systems in…Z-1857-2024
May 29, 2024FDASmartPath to dStream for 3.0T Model Number (REF): 782145Z-1861-2024
May 29, 2024FDASmartPath to Ingenia Elition X - Magnetic Resonance (MR) systems are Medical Electrical S…Z-1863-2024
May 29, 2024FDAAchieva 1.5T Conversion- Magnetic Resonance (MR) systems are Medical Electrical Systems i…Z-1837-2024
May 29, 2024FDAAchieva 3.0T TX for PET Model Number (REF): 781479Z-1841-2024
May 29, 2024FDAAchieva 1.5T Initial system Model Number (REF): 781178Z-1838-2024
May 29, 2024FDAPanorama HFO- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated fo…Z-1855-2024
May 29, 2024FDAAchieva 3.0T Model Number (REF): (1) 781345; (2) 781344; (3) 781278; (4) 781277; …Z-1839-2024

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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