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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

589

Class I (Serious)

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 3981–4000 of 10393 recalls

Incisive CT X-ray System (Philips) – Table Movement Issue (2020)

Patient tabletop moved out to the home position during scan initialization, may cause operator/bystander staying by the rear of the table to collide with the moved tabletop and be injured

Moderate

FDADec 24, 2020Nationwide• Philips North America

Excedrin Migraine Caplets (GSK) – Packaging Safety (2020)

This recall involves 50, 80, 100, 125, 200, 250 and 300-count bottles of Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets. The bottles are plastic with a child-resistant closure. For a full list of the recalled products, visit www.excedrin.com/products/discontinued.

Low

CPSCDec 23, 2020Nationwide• GSK Consumer Healthcare, of Warren, N.J.

PSG-1100 Sleep System (Nihon Kohden) – Safety Standard Issue (2020)

Medical device non-conformance to electrical safety standard (IEC 60601-1).

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Moderate

FDADec 21, 2020Nationwide• Nihon Kohden America Inc

ONE-LINK Catheter Set (Baxter) – Tubing Separation (2020)

There were customer reports of separation between the tubing and Male Luer Lock Adaptor.

Moderate

FDADec 21, 2020Nationwide• Baxter Healthcare Corporation

Hurricane Motorhome (Thor) – Cabinet Safety Issue (2020)

Thor Motor Coach (TMC) is recalling certain 2018-2019 Hurricane and Windsport motorhomes. The overhead cabinets located above the driver and front passenger seats may detach and fall onto the seat occupants, possibly causing the driver to lose control of the vehicle.

Moderate

NHTSADec 21, 2020Nationwide• THOR MOTOR COACH

Zerbaxa Injection (Merck) – Sterility Concern (2020)

Lack of assurance of sterility: The results of sterility tests of seven batches of product were out of specification. Five of these batches tested positive for Ralstonia pickettii and two batches produced turbid results that could not be further identified. While all product distributed to the market has met the registered specifications for release, including for sterility, it was manufactured on the same equipment as the affected batches.

Class IIModerate

FDADec 21, 2020Nationwide• Merck Sharp & Dohme

VERSABOND AB Bone Cement (Smith & Nephew) – Consistency Problem (2020)

Potential heat and humidity exposure. The affected lot contained an atypical sandy, flaky or grainy consistency when mixing.

Moderate

FDADec 18, 2020Nationwide• Smith & Nephew, Inc.

Compact Suction Unit (Laerdal) – Suction Loss Risk (2020)

Component failures may cause the unit to lose all suction. Users will need to obtain alternate suction devices or methods, leading to a delay in treatment and, in worst case scenario, potential suffocation if alternative suction or ventilation method is not administered by the user.

Very High

FDADec 18, 2020Nationwide• Laerdal Medical (Suzhou) Co., Ltd. Science & Technology Ind. Park No.

Revolution CT System (GE Healthcare) – Potential System Issue (2020)

Laceration Risk

GE Healthcare has become aware of a potential issue on Revolution Apex, Revolution CT with Apex Edition, Revolution CT, and Revolution CT ES systems where the table pinch protector could be damaged or missing leading to exposed table screws which could cause a laceration due to a sharp edge.

High

FDADec 17, 2020Nationwide• GE Healthcare, LLC

Almond Danish Kringle (O&H Danish Bakery) – Undeclared Pecans (2020)

Undeclared Allergen

Almond Kringle may contain undeclared Pecans.

Class IIModerate

FDADec 17, 2020AL, AR, CO +7 more• O & H DANISH BAKERY

VERITAS Collagen Matrix (Baxter) – Undersized Dimensions (2020)

VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.

Low

FDADec 11, 2020Nationwide• Baxter Healthcare Corporation

Homfa Cabinets (Shenzhen Luosi Ge) – Tip-Over Risk (2020)

This recall involves the Homfa HPB-087 and HPB-106 cabinets. The HPB-087 was sold in walnut brown and the HPB-106 was sold in wood grain. The cabinets measure about 29.75 inches tall, 31.5 inches wide, and 15.4 inches deep and weigh about 59 pounds.

High

CPSCDec 10, 2020Nationwide• Shenzhen Luosi Ge Trading Co., of China (owner of Homfa trademark)

Discovery NM Systems (GE Healthcare) – Rotor Bearing Problem (2020)

GE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.

Moderate

FDADec 10, 2020Nationwide• GE Healthcare, LLC

NM/CT 860 System (GE Healthcare) – Rotor Bearing Issue (2020)

GE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.

Moderate

FDADec 10, 2020Nationwide• GE Healthcare, LLC

NM/CT 850 System (GE Healthcare) – Rotor Bearing Concern (2020)

GE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.

Moderate

FDADec 10, 2020Nationwide• GE Healthcare, LLC

Precision 600FP System (GE Healthcare) – Monitor Suspension Risk (2020)

GE Healthcare has become aware of a potential safety issue associated with the improper installation of the Precision 600FP monitor suspension. A partial detachment of the monitor suspension could result in potential injury to a patient or operator.

High

FDADec 10, 2020Nationwide• GE Healthcare, LLC

NM/CT 870 CZT System (GE Healthcare) – Rotor Bearing Issue (2020)

GE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.

Moderate

FDADec 10, 2020Nationwide• GE Healthcare, LLC

Optima NM/CT 640 (GE Healthcare) – Rotor Bearing Problem (2020)

GE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.

Moderate

FDADec 10, 2020Nationwide• GE Healthcare, LLC

Discovery NM Systems (GE Healthcare) – Rotor Bearing Concern (2020)

GE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.

Moderate

FDADec 10, 2020Nationwide• GE Healthcare, LLC

Western Chief Toddler Boots – Choking Hazard (2020)

Choking Hazard

This recall includes the Western Chief "Abstract Camo," "Alia Silver," and "Sweetheart Navy" Light-Up Rain Boots in sizes 5-12 for toddlers or children. The recalled boots are camouflage, silver glitter, and navy with hearts; include boot handles; and have a light up feature in the heel of the boot. The rivets used to attach the handles are silver-gray in color. "Western Chief" and the model numbers are located on the inside tag of the boot. The recalled model numbers are T24121725P, T24121728P, and T24121729P.

Moderate

CPSCDec 9, 2020Nationwide• Washington Shoe Company, of Kent, Wash.