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Philips North America

Philips North America Recalls

All product recalls associated with Philips North America.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

34

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 2941–2960 of 21320 recalls

BrightView X Gamma Camera (Philips) – Detector Fall Risk (2023)

Laceration Risk

Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation.

FDADec 15, 2023Nationwide• Philips North America

IgM Total Test (Siemens) – Potential Negative Bias (2023)

Potential for a negative bias with quality control (QC) and patient sample results when using the Atellica CH Immunoglobulin M_2 (IgM_2) reagent.

FDADec 15, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

Panther Fusion System (Hologic) – False Flu B Result (2023)

Due to potential false positive Flu B results when a sample was also SARS-CoV-2 positive.

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High

FDADec 15, 2023Nationwide• Hologic, Inc.

Banana Foster Bar (ToYou Snacks) – Undeclared Soy (2023)

Undeclared Allergen

Undeclared Soy Allergen in various fruit and chocolate snack bars

Class IIModerate

FDADec 15, 2023Nationwide• Font Group of America Corp.

Coconut Mocha Snack Bar (ToYou) – Undeclared Soy (2023)

Undeclared Allergen

Undeclared Soy Allergen in various fruit and chocolate snack bars

Class IIModerate

FDADec 15, 2023Nationwide• Font Group of America Corp.

Chocolate Mango Bar (Font Group) – Undeclared soy (2023)

Undeclared Allergen

Undeclared Soy Allergen in various fruit and chocolate snack bars

Class IIModerate

FDADec 15, 2023Nationwide• Font Group of America Corp.

Mint Dark Chocolate Bar (Font Group) – Undeclared soy (2023)

Undeclared Allergen

Undeclared Soy Allergen in various fruit and chocolate snack bars

Class IIModerate

FDADec 15, 2023Nationwide• Font Group of America Corp.

Salted Caramel Dark Chocolate Bar (ToYou) – Undeclared Soy (2023)

Undeclared Allergen

Undeclared Soy Allergen in various fruit and chocolate snack bars

Class IIModerate

FDADec 15, 2023Nationwide• Font Group of America Corp.

Mango Yogurt Bar (ToYou) – Undeclared Soy (2023)

Undeclared Allergen

Undeclared Soy Allergen in various fruit and chocolate snack bars

Class IIModerate

FDADec 15, 2023Nationwide• Font Group of America Corp.

Pneumonia Panel Plus (BioFire) – False Positive Risk (2023)

Their is a potential for false positive results when using Pneumonia panel.

FDADec 14, 2023Nationwide• BioFire Diagnostics, LLC

Can-Am Side-By-Side Vehicles (BRP) – Injury Hazard (2023)

This recall involves Model Year 2022 and 2023 Can-Am Commander series, Defender series, Maverick Trail series equipped with an HD7 or 700 engines side-by-side vehicles with model number model year 2022 and 2023. The vehicles were sold in various colors. The brand and model name are on the vehicle's sides.

CPSCDec 14, 2023Nationwide• BRP Mexico, of Mexico

Pneumonia Panel (BioFire) – False Positive Risk (2023)

Their is a potential for false positive results when using Pneumonia panel.

FDADec 14, 2023Nationwide• BioFire Diagnostics, LLC

Spectral CT on Rails (Philips) – Image Labeling Error (2023)

A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.

FDADec 13, 2023Nationwide• PHILIPS MEDICAL SYSTEMS

Spectral CT 7500 (Philips) – Image Labeling Error (2023)

A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.

FDADec 13, 2023Nationwide• PHILIPS MEDICAL SYSTEMS

VACUETTE Blood Tube (Greiner) – Additive Missing Concern (2023)

Tubes have missing additive/anticoagulant resulting in clotting in most cases. A completely clotted sample would lead to no results being reported, which could lead to a delay in treatment or diagnosis. An erroneous glucose or lactose result from a partially clotted sample could lead to inappropriate treatment.

FDADec 12, 2023Nationwide• Greiner Bio-One North America, Inc.

Azurion System (Philips) – Imaging Functionality Loss (2023)

System may exhibit a loss of imaging functionality and data due to an issue which can cause the system to continuously restart. If the issue occurs during a procedure, there may be a delay and/or abortion of the procedure.

FDADec 12, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

TECNIS Toric II IOL (Johnson & Johnson) – Angle Specification Issue (2023)

Due to intraocular lens containing an angle out of specification (OOS). The cylinder axis marks do not meet product specifications for the allowable angle between Low Power Meridian (LPM) and toric cylinder axis marks.

FDADec 12, 2023Nationwide• Johnson & Johnson Surgical Vision, Inc.

Paparrela-Type Vent Tube (Olympus) – Expiration Date Missing (2023)

The expiration date is missing from the primary (inner) packaging. The secondary (outer) box label correctly states the expiration date of February 12, 2033, for this lot

FDADec 11, 2023Nationwide• Olympus Corporation of the Americas

Cranial Drill 2.40mm (Globus) – Sterility Packaging Concern (2023)

Sterile-packed Cranial Drills may not be sterile due to a breach in the packaging and/or may have discoloration near the drill tip.

FDADec 11, 2023Nationwide• Globus Medical, Inc.

Cranial Drill 6.00mm (Globus) – Sterility Packaging Concern (2023)

Sterile-packed Cranial Drills may not be sterile due to a breach in the packaging and/or may have discoloration near the drill tip.

FDADec 11, 2023Nationwide• Globus Medical, Inc.