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Philips North America Llc

Philips North America Llc Recalls

All product recalls associated with Philips North America Llc.

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Recall Summary

Total Recalls

532

Past Year

77

Class I (Serious)

0

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 181–200 of 532 recalls

Philips North America Llc: Intera Achieva 1.5T Pulsar, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

Philips North America Llc: Intera 1.5T Master/Nova, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

Philips North America Llc: Achieva 1.5T Conversion, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

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Philips North America Llc: Evolution Upgrade 3.0T, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

Philips North America Llc: Achieva XR, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

Philips North America Llc: Achieva 3.0T for PET, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

Philips North America Llc: MR 5300, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

Philips North America Llc: Ingenia Elition X, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

Philips North America Llc: Achieva 3.0TX for PET, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

Philips North America Llc: Ingenia Elition S, Magnetic Resonance System.

Patient support table floor plate may be incorrectly installed.

FDAMar 12, 2024Nationwide• Philips North America Llc

Philips North America: CareEvent Event Management System, Model Numbers 866435 a...

It was found that the Care Assist mobile application (version 4.1.1 and earlier) would not play custom ringtones when iOS device screens were locked with a passcode.

FDAFeb 28, 2024Nationwide• Philips North America

Philips North America: Patient Information Center iX (PIC iX), Model Numbers 866...

It was found that the Care Assist mobile application (version 4.1.1 and earlier) would not play custom ringtones when iOS device screens were locked with a passcode.

FDAFeb 28, 2024Nationwide• Philips North America

Philips North America Llc: DIVA 24 Inch Widescreen LCD Touch Display - Used with the...

If the DIVA touch display generates touch inputs without user interaction, due to possibility of the erroneous acknowledgement of a patient alarm, there is a potential for a delay in the detection of a change in a patient condition which prompted the alarm to generate. Although unlikely, this could potentially result in a patient harm.

FDAFeb 15, 2024Nationwide• Philips North America Llc

Philips North America: Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261.

Laceration Risk

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

FDAJan 3, 2024Nationwide• Philips North America

Philips North America: Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.

Laceration Risk

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

FDAJan 3, 2024Nationwide• Philips North America

Philips North America: SmartPath to dStream for XR and 3.0T. Model (REF) Numbers...

Laceration Risk

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

FDAJan 3, 2024Nationwide• Philips North America

Philips North America: Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283.

Laceration Risk

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

FDAJan 3, 2024Nationwide• Philips North America

Philips North America: Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.

Laceration Risk

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

FDAJan 3, 2024Nationwide• Philips North America

Philips North America: Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278...

Laceration Risk

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

FDAJan 3, 2024Nationwide• Philips North America

Philips North America: Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105.

Laceration Risk

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

FDAJan 3, 2024Nationwide• Philips North America