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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

1000

Past Year

589

Class I (Serious)

65

Most Recent

Jan 2026

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 4641–4660 of 10393 recalls

Integris Allura X-Ray System (Philips) – capacitor failure (2019)

A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.

FDADec 30, 2019Nationwide• Philips North America, LLC

Allura Exper FD Series (Philips) – capacitor failure (2019)

A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.

FDADec 30, 2019Nationwide• Philips North America, LLC

MultiDiagnost Eleva (Philips) – capacitor failure (2019)

A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.

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FDADec 30, 2019Nationwide• Philips North America, LLC

Poly G Integris H5000 (Philips) – capacitor failure (2019)

A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.

FDADec 30, 2019Nationwide• Philips North America, LLC

Allura CV20 (Philips) – capacitor failure (2019)

A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.

FDADec 30, 2019Nationwide• Philips North America, LLC

OmniDiagnost Eleva (Philips) – capacitor failure (2019)

A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.

FDADec 30, 2019Nationwide• Philips North America, LLC

WRIGHT EVOLVE Proline Head (Wright Medical) – incorrect sizing (2019)

Two lots of EVOLVE Modular Radial Head could have the wrong size product in the package. Both the label and laser marking are incorrect on the affected product.

FDADec 27, 2019Nationwide• Wright Medical Technology, Inc.

RTE Bacon and Eggs (Cheesewich Factory) – Listeria Contamination (2019)

Eggs in RTE bacon and egg packet may contain Listeria Monocytogenes.

FDADec 27, 2019IL, MI, NC• Cheesewich Factory

Kangaroo Epump Spike (Cardinal Health) – potential leakage (2019)

The feeding spike sets may leak at the interface of the tube and spike connector.

FDADec 26, 2019Nationwide• Cardinal Health Inc.

Kangaroo 924 Spike Set (Cardinal Health) – potential leakage (2019)

The feeding spike sets may leak at the interface of the tube and spike connector.

FDADec 26, 2019Nationwide• Cardinal Health Inc.

Kangaroo ENPlus Spike Set (Cardinal Health) – potential leakage (2019)

The feeding spike sets may leak at the interface of the tube and spike connector.

FDADec 26, 2019Nationwide• Cardinal Health Inc.

Kangaroo Joey Spike (Cardinal Health) – potential leakage (2019)

The feeding spike sets may leak at the interface of the tube and spike connector.

FDADec 26, 2019Nationwide• Cardinal Health Inc.

Protein Trail Mix (H.T. Hackney) – Listeria Contamination (2019)

Product potentially contaminated with Listeria monocytogenes.

FDADec 24, 2019AL, GA, IN +5 more• The H.T. Hackney Co. LLC

Protein Snack Tray (H.T. Hackney) – Listeria Contamination (2019)

Product potentially contaminated with Listeria monocytogenes.

FDADec 24, 2019AL, GA, IN +5 more• The H.T. Hackney Co. LLC

SIGNA Vibrant MRI System (GE Healthcare) – incorrect date setting (2019)

It was identified that due to a potential installation workflow issue, the MR system date could be set incorrectly. The system s date and time setting are used to populate the DICOM header information on images. This could result is an inaccurate date recorded on the images.

FDADec 23, 2019Nationwide• GE Healthcare, LLC

SIGNA Architect MRI System (GE Healthcare) – incorrect date setting (2019)

It was identified that due to a potential installation workflow issue, the MR system date could be set incorrectly. The system's date and time setting are used to populate the DICOM header information on images. This could result is an inaccurate date recorded on the images.

FDADec 23, 2019Nationwide• GE Healthcare, LLC

VesselNavigator (Philips) – DSA export problem (2019)

Due to a software defect, when a digital subtraction angiography (DSA) is exported to the VesselNavigator application, the DSA is displayed without subtraction.

FDADec 23, 2019Nationwide• Philips North America, LLC

SIGNA Premier MRI System (GE Healthcare) – incorrect date setting (2019)

It was identified that due to a potential installation workflow issue, the MR system date could be set incorrectly. The system's date and time setting are used to populate the DICOM header information on images. This could result is an inaccurate date recorded on the images.

FDADec 23, 2019Nationwide• GE Healthcare, LLC

SIGNA Pioneer MRI System (GE Healthcare) – incorrect date setting (2019)

It was identified that due to a potential installation workflow issue, the MR system date could be set incorrectly. The system's date and time setting are used to populate the DICOM header information on images. This could result is an inaccurate date recorded on the images.

FDADec 23, 2019Nationwide• GE Healthcare, LLC

Theraflu Cough Relief (GSK) – Missing Warning Label (2019)

Labeling: Label Lacks Warning: Product recalled due to absence of a warning statement on the product label, Ask a doctor before use if you have a sodium-restricted diet.

Class IIModerate

FDADec 23, 2019Nationwide• GSK Consumer Health, Inc