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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

1000

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 2641–2660 of 21320 recalls

Ingenia Elition S (Philips) – Floor Plate Installation Error (2024)

Patient support table floor plate may be incorrectly installed.

High

FDAMar 12, 2024Nationwide• Philips North America Llc

Door County Chocolate Cherry Granola (Kick Ash) – Undeclared Almond (2024)

Undeclared Allergen

Undeclared allergen (almond) in Dark Chocolate Cherry Granola

Class IHigh

FDAMar 12, 2024IL, IN, WI• Kick Ash Products LLC

RENASYS EDGE 300ML Canister (Smith & Nephew) – Carbon Filter Contamination (2024)

Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump

Moderate

1...131 132133134 135...1066

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FDA

Mar 11, 2024

Nationwide

• Smith & Nephew Medical, Ltd.

RENASYS EDGE 800ML Canister (Smith & Nephew) – Carbon Filter Contamination (2024)

Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump

Moderate

FDAMar 11, 2024Nationwide• Smith & Nephew Medical, Ltd.

Galaxy System (Noah Medical) – Wired Controller Misalignment (2024)

Due to a misaligned calibration of the wired controller that may result in unintended motion of the scope.

High

FDAMar 9, 2024Nationwide• Noah Medical

Zero Sugar Ginger Ale (Pepsico) – Sugar Mislabeling (2024)

During an internal investigation the firm discovered that product labeled as Zero Sugar contains full sugar product.

Class IIModerate

FDAMar 9, 2024MD, PA, WV• Pepsico Inc

STRATAFIX Spiral MONOCRYL Plus (Ethicon) – Sterility Compromise (2024)

Degraded and unusable upon removal from the foil pouch due to exposed environmental conditions during transit and storage, compromising sterility

High

FDAMar 8, 2024CO, GA, IA +6 more• Ethicon, Inc.

PowerSeal 5mm Curved Jaw Sealer (Olympus) – Incomplete Seal Cycle (2024)

Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.

High

FDAMar 7, 2024Nationwide• Olympus Corporation of the Americas

PowerSeal 44cm Curved Jaw Sealer (Olympus) – Incomplete Seal Cycle (2024)

High

FDAMar 7, 2024Nationwide• Olympus Corporation of the Americas

Bracelet (Skechers) – High Lead Levels (2024)

This recall involves the braided black bracelet that is a part of the Skechers watch/bracelet gift set. The bracelet is black and features a braided pattern with a metal clasp on each end. The watch in the gift set has a code number "IF2812307" printed on the back of the watch as well as "Sketchers" and model number "SR9082".

Very High

CPSCMar 7, 2024Nationwide• Fossil Group Inc., of Richardson, Texas

Arctic Cat Catalyst Snowmobiles (Textron) – Injury Risk (2024)

This recall involves all model year 2024 Arctic Cat Catalyst 600 series snowmobiles. The snowmobiles were sold in various colors and model name "ZR," "Riot" or "Mountain" printed on each side of the engine cowling.

High

CPSCMar 7, 2024Nationwide• Textron Specialized Vehicles, of Augusta, Georgia

Tri-Lo-Sprintec (Teva) – dissolution failure (2024)

Failed Dissolution Specifications

Class IIModerate

FDAMar 7, 2024Nationwide• Teva Pharmaceuticals USA, Inc

PowerSeal 37cm Curved Jaw Sealer (Olympus) – Incomplete Seal Cycle (2024)

High

FDAMar 7, 2024Nationwide• Olympus Corporation of the Americas

KWIK-STIK Rhizopus Stolonifer (Microbiologics) – Fungal Contamination (2024)

The positive control material (Rhizopus stolonifer) within the KWIK-STIK assembly was contaminated with another fungal organism (Aspergillus brasiliensis). As a result, users may observe A. brasiliensis growth when using the control material.

Moderate

FDAMar 6, 2024Nationwide• Microbiologics Inc

Tablo Hemodialysis System (Outset Medical) – Tubing Replacement (2024)

Hemodialysis System, pre and post dialyzer peroxide-cured silicone tubing, with less than 336 hours usage, will be replaced because tubing may contain non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs), that have not been flushed out over time with usage. Exposure to PCBAs could cause: skin conditions, liver damage, impaired reproduction, development of certain kinds of cancer in humans.

High

FDAMar 6, 2024AL, AK, AZ +39 more• Outset Medical, Inc.

Potassium Chloride Injection (B. Braun) – sterility risk (2024)

Lack of assurance of sterility: pinholes, within the blue label characters on the EXCEL bag, specifically within the dotted characters on the label, resulting in leaks.

Class IIModerate

FDAMar 6, 2024Nationwide• B. Braun Medical Inc

Infinity Resection Adjustment Block (Wright Medical) – Manufacturing Defect (2024)

Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument assembly. The missing screw is used to lockout the Medial/Lateral adjustment on the INFINITY Resection Adjustment Guide.

Moderate

FDAMar 6, 2024NE, TX• Wright Medical Technology, Inc.

OptiCross Coronary Imaging Catheter (Boston Scientific) – Image Quality Issue (2024)

Certain batches of Opticross 40MHz Coronary Imaging Catheters manufactured using an incorrect voltage setting, which may have resulted in decreased image brightness.

Moderate

FDAMar 5, 2024Nationwide• Boston Scientific Corporation

Neria Soft Infusion Set (Unomedical) – Incorrect Instructions (2024)

Specific lots of Neria Soft Infusion Sets, which have been shipped into the US Market, have been shipped with the incorrect Instruction for Use (IFU) within the final pack. The IFU included is the IFU registered for the Rest of World (ROW) countries. The difference between the US IFU and the ROW IFU is the addition of an intended use section in the ROW IFU.

Low

FDAMar 5, 2024Nationwide• Unomedical A/S Osted Aholmvej 1

NEOMED Pharmacy Syringes (Avanos) – Expiration Date Omission (2024)

The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.

Low

FDAMar 4, 2024Nationwide• Avanos Medical, Inc.