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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M12; Catalog numbers: (1) 722227, (2) 722231 (OUS ONLY).
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M15; Catalog numbers: (1) 722064, (2) 722222 (3) 722280(OUS ONLY).
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M12; Catalog numbers: (1) 722063, (2) 722221.
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C; Catalog number: 722001
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura CV20; Catalog numbers: 722031
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; Catalog numbers: 722038
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15; Catalog numbers: 722058
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; Catalog numbers: 722029
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 OR Table; Catalog numbers: (1) 722023, (2) 722035.
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane OR Table; Catalog numbers: (1) 722020, (2) 722025.
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013.
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10/10; Catalog numbers: (1) 722005, (2) 722011, (3) 722027.
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,
Hazard: Possibility of the patient falling from the table related to the mattress used on the patient table.
February 26, 2025Medical DevicesFDA
Spectranetics Corporation recalls Intact Vascular Tack Endovascular System, to treat vascular dissections with Tack implant(s) following angioplasty: (4F,
Hazard: Use of Tack Endovascular system, designed to treat acute dissections of inner wall or lining of an artery by tacking damaged tissue to inner luminal surface, could result in problems with deployment and stability of device in vessel after deployment, which may cause failure to resolve dissection, migration of implant, bailout stenting, reintervention, unintended removal of tack devices, and ischemia.
February 26, 2025Food & BeverageFDA
United Natural Trading Inc. dba Woodstock Farms recalls Wegmans, Organic Almonds Dry Roasted Salted, 12oz clear bag, 12 bags per case.
Hazard: Product mislabeled. The back label states Organic Cashews. The front product label states Wegmans Organic unsalted dry roasted almonds. The front label is correct label for this product.
February 26, 2025Food & BeverageFDA
Robin J Vos dba TS Food Packaging recalls Bacon flavored Popcorn Seasoning packaged under the following brands and sizes: 1. Wabash Valley Farms, Net Wt. 4.2 o
Hazard: Undeclared allergen (soy).
February 26, 2025Food & BeverageFDA
Jack & The Green Sprouts, Inc. recalls Jack & the Green Sprouts Alfalfa Sprouts. Net Weight 5 oz. (152g). UPC 7 63247-19891 5. Keep Refrigerated. Product
Hazard: Sprouts have the potential to be contaminated with Listeria monocytogenes
February 26, 2025Food & BeverageFDA
Global Commodities Inc recalls AAHU BARAH brand SOFT PLUM; NET WT. 0.5 LB; Import By: AAHU BARAH USA, INC.; Soft Plum Aloo Bukahara 1/2 LB; *May Contai
Hazard: Product contains undeclared sulfites (4.66 mg/serving).
February 26, 2025Food & BeverageFDA
NEW YORK WHOLESALE GROUP recalls ZAARAH HERBALS brand SHATAVARI POWDER; 100% ASPARAGUS RACEMOSUS; (Supports Female Reproductive System); Supreme Fine Pow
Hazard: Product contains elevated levels of lead - 6.50 mg/kg (ppm)
February 26, 2025Food & BeverageFDA
FEEL GOOD FOODS INC recalls Feel Good Foods; Three Cheese Mac & Cheese Bites; NET WT 8oz (224g); packaged in yellow carton; 9 units per case; Frozen
Hazard: Foreign object (metal pieces).
February 26, 2025Food & BeverageFDA
Shata Traders Inc. recalls THREE RIVERS brand TUTTI-FRUTTI; INGREDIENTS Papaya Cubes, Sugar, Citric Acid (E-330), Potassium Sorbate (E-202), FD&C R
Hazard: Product contains undeclared FD&C Yellow 5 and FD&C Yellow 6.
February 26, 2025Food & BeverageFDA
Apna Wholesale Inc. recalls Paras Premium Golden Raisins; 7 oz and 14 oz; INGREDIENTS: RAISINS; ALLERGEN STATEMENT: Processed in a gluten-free and p
Hazard: Product contains undeclared sulfites (56.8mg/serving)
February 26, 2025DrugsFDA
Alvogen, Inc recalls Fentanyl Transdermal System CII, 25mcg/h, packaged in a pouch, further packaged in 5-count carton, Rx only, Distributed
Hazard: Defective delivery system - patches could be multi-stacked, adhered one on top of the other, in a single product pouch.
February 26, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Atomoxetine Capsules, USP, 100 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141,
Hazard: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
February 26, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Atomoxetine Capsules, USP, 80 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, M
Hazard: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
February 26, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Atomoxetine Capsules, USP, 60 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, M
Hazard: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
February 26, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Atomoxetine Capsules, USP, 40 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, M
Hazard: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
February 26, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Atomoxetine Capsules, USP, 25 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, M
Hazard: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
February 26, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Atomoxetine Capsules, USP, 18 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, M
Hazard: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.