Philips North America recalls
Philips North America appears in 532 official U.S. recall notices indexed by RecallRadar.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Mammotrak Diagnostic Coil 1.5T
FDA Device · Class II · 2024-12-04 · Philips North America - dS Breast 16ch 3.0T
FDA Device · Class II · 2024-12-04 · Philips North America - dS Breast 16ch 1.5T
FDA Device · Class II · 2024-12-04 · Philips North America - SENSE Breast Coil 3.0T 7ch
FDA Device · Class II · 2024-12-04 · Philips North America - ST SENSE Breast Dx Coil
FDA Device · Class II · 2024-12-04 · Philips North America - IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Option CP2 are affected as follows: 1) In…
FDA Device · Class II · 2024-10-16 · Philips North America - Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390, Software Revision 4.0.1
FDA Device · Class II · 2024-10-16 · Philips North America - IntelliVue G7m Anesthesia Gas Module, Product Number 866173
FDA Device · Class II · 2024-10-09 · Philips North America - DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system central monitoring system
FDA Device · Class II · 2024-10-09 · Philips North America - Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal stru…
FDA Device · Class II · 2024-10-02 · Philips North America - IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX450 (Model Number 866062), MX500 (Model Number 86606…
FDA Device · Class II · 2024-10-02 · Philips North America - Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structu…
FDA Device · Class II · 2024-10-02 · Philips North America - Ingenia Ambition S - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal s…
FDA Device · Class II · 2024-10-02 · Philips North America - Ingenia Ambition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal s…
FDA Device · Class II · 2024-10-02 · Philips North America - SmartPath to Ingenia Elition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of th…
FDA Device · Class II · 2024-10-02 · Philips North America - SmartPath to dStream for XR and 3.0T- For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra…
FDA Device · Class II · 2024-10-02 · Philips North America - Evolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the intern…
FDA Device · Class II · 2024-10-02 · Philips North America - MR 7700 -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of…
FDA Device · Class II · 2024-10-02 · Philips North America - Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structur…
FDA Device · Class II · 2024-10-02 · Philips North America - SmartPath to dStream for 1.5T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the…
FDA Device · Class II · 2024-10-02 · Philips North America - Ingenia Elition X- For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal str…
FDA Device · Class II · 2024-10-02 · Philips North America - MR 5300 - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of…
FDA Device · Class II · 2024-10-02 · Philips North America - Ingenia Elition S -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal str…
FDA Device · Class II · 2024-10-02 · Philips North America - IntelliVue Patient Monitor MX400 with L.x and M.x
FDA Device · Class II · 2024-08-14 · Philips North America - IntelliVue Patient Monitor MX550 with L.x and M.x
FDA Device · Class II · 2024-08-14 · Philips North America - IntelliVue Patient Monitor MX500 with L.x and M.x
FDA Device · Class II · 2024-08-14 · Philips North America - IntelliVue Patient Monitor MX450 with L.x and M.x
FDA Device · Class II · 2024-08-14 · Philips North America - Avalon Ultrasound Transducer
FDA Device · Class II · 2024-07-10 · Philips North America - SENSE XL TORSO COIL 1.5T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems
FDA Device · Class I · 2024-07-03 · Philips North America - SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems
FDA Device · Class I · 2024-07-03 · Philips North America - SENSE XL TORSO COIL 3.0T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems
FDA Device · Class I · 2024-07-03 · Philips North America - HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100064…
FDA Device · Class II · 2024-06-12 · Philips North America - HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100064…
FDA Device · Class II · 2024-06-12 · Philips North America - HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100…
FDA Device · Class II · 2024-06-12 · Philips North America - Evolution upgrade 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Numbe…
FDA Device · Class II · 2024-05-29 · Philips North America - SmartPath to dStream for XR and 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic devi…
FDA Device · Class II · 2024-05-29 · Philips North America - SmartPath to dStream for 3.0T Model Number (REF): 782145
FDA Device · Class II · 2024-05-29 · Philips North America - AchievaXR -Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 7812…
FDA Device · Class II · 2024-05-29 · Philips North America - Achieva 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): (…
FDA Device · Class II · 2024-05-29 · Philips North America - Marlin 1.5T - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2024-05-29 · Philips North America - Sonalleve MR HIFU 3.0T - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2024-05-29 · Philips North America - MR 5300- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2024-05-29 · Philips North America - Ingenia 1.5T Model Number (REF): (1) 782140
FDA Device · Class II · 2024-05-29 · Philips North America - Achieva 1.5T Initial system Model Number (REF): 781178
FDA Device · Class II · 2024-05-29 · Philips North America - Ingenia Ambition S Model Number (REF): (1) 782139
FDA Device · Class II · 2024-05-29 · Philips North America - Incisive CT - Computed Tomography X-Ray System intended to produce cross-sectional images of the body
FDA Device · Class II · 2024-05-29 · Philips North America - Ingenia 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2024-05-29 · Philips North America - Intera 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2024-05-29 · Philips North America - Ingenia Elition X- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2024-05-29 · Philips North America - Ingenia 1.5T S Model Number (REF): 781347
FDA Device · Class II · 2024-05-29 · Philips North America