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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
April 15, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringe
Hazard: Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
April 15, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringe
Hazard: Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
April 15, 2026Medical DevicesFDA
Medline Industries, LP recalls NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007;
Hazard: Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
April 15, 2026Medical DevicesFDA
Medline Industries, LP recalls NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10M
Hazard: Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
April 15, 2026Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.
Hazard: During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing significantly higher, the actual applied x-ray dose levels are in accordance with the system settings and imaging conditions, as well as the applicable regulatory requirements.
April 15, 2026Food & BeverageFDA
AYCO FARMS INC recalls Fresh Cantaloupe (Whole, Fresh), brand name Ayco, wrapped in food safe plastic bags packed in corrugated cardboard carto
Hazard: Potential Salmonella Contamination
April 15, 2026Food & BeverageFDA
Blueroot Health, Inc. recalls Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count b
Hazard: Contains undeclared egg, soy, and hazelnut
April 15, 2026Food & BeverageFDA
Riverence Provisions LLC recalls Riverence Smoked Trout Dip, net wt. 7oz. Product is perishable, refrigerated, packaged in plastic tub. Product is shippe
Hazard: Label declares cream cheese but does not declare milk
April 15, 2026Food & BeverageFDA
F&S Fresh Foods, Inc. recalls ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, perishable, Keep Refrigerated, plastic clamshell, net wt. 10 oz,
Hazard: Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.
April 15, 2026Food & BeverageFDA
MEI YU CHENG DA TRADING INC recalls Olive Skewers individually wrapped and packaged in clear plastic bag; 500g; INGREDIENTS: Olive, edible salt, white sugar
Hazard: Products contain banned sweetener: cyclamates.
April 15, 2026Food & BeverageFDA
MEI YU CHENG DA TRADING INC recalls DADI NONGFU DRIED SALT CHILLI VEGETABLE(S); Ingredients: Radish, chili, roasted sesame, prickly ash, edible salt, soybea
Hazard: Products contain banned sweetener: cyclamates.
April 15, 2026Food & BeverageFDA
Connecticut Crab Company LLC recalls Crab Cakes various sizes sold to food service
Hazard: May be temperature abused, which may result in growth of Clostridium botulinum
April 15, 2026Food & BeverageFDA
Pure Vitamins and Natural Supplements, LLC recalls Red Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entir
Hazard: FDA analysis revealed the presence of undeclared sildenafil
April 15, 2026Food & BeverageFDA
Pure Vitamins and Natural Supplements, LLC recalls Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Enti
Hazard: FDA analysis revealed the presence of undeclared sildenafil
April 15, 2026Food & BeverageFDA
Pure Vitamins and Natural Supplements, LLC recalls Boner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: C
Hazard: FDA analysis revealed the presence of undeclared sildenafil and Tadalafil
April 15, 2026Food & BeverageFDA
Zarlengo Italian Ice recalls Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon bucket/pail - white round food and freezer grade High-Densi
Hazard: Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
April 15, 2026Food & BeverageFDA
Zarlengo Italian Ice recalls Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/p
Hazard: Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
April 15, 2026Food & BeverageFDA
Zarlengo Italian Ice recalls Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gal
Hazard: Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
April 15, 2026DrugsFDA
Teva Pharmaceuticals USA, Inc recalls Clonidine Transdermal System, USP, 0.3 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only, Manufact
Hazard: CGMP Deviations: use of an unapproved raw material
April 15, 2026DrugsFDA
Teva Pharmaceuticals USA, Inc recalls Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only, Manufact
Hazard: CGMP Deviations: use of an unapproved raw material
April 15, 2026DrugsFDA
Teva Pharmaceuticals USA, Inc recalls Clonidine Transdermal System, USP, 0.1 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx Only, Manufact
Hazard: CGMP Deviations: use of an unapproved raw material
April 15, 2026DrugsFDA
GE Healthcare Ireland Limited recalls GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough
Hazard: Presence of particulate matter
April 15, 2026DrugsFDA
GE Healthcare Ireland Limited recalls GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough
Hazard: Presence of particulate matter
April 15, 2026DrugsFDA
Teva Pharmaceuticals USA, Inc recalls Isotretinoin Capsules, USP, 40 mg, 10 count Prescription Pacs, Rx only, Manufactured for: Teva Pharmaceuticals USA, Inc.
Hazard: Superpotent and Subpotent
April 15, 2026DrugsFDA
Teva Pharmaceuticals USA, Inc recalls Isotretinoin Capsules, USP, 30 mg, Rx Only, 10 count Prescription Pack, Manufactured for: Teva Pharmaceuticals USA, Inc.
Hazard: Superpotent and Subpotent
April 15, 2026DrugsFDA
Viatris, Inc. recalls Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty LLC
Hazard: Failed Dissolution Specifications
April 15, 2026DrugsFDA
Preferred Pharmaceuticals, Inc. recalls Artificial Tears Lubricant Eye Drops (glycerin 0.2%, hypromellose 0.2%, polyethylene glycol 400 1%), 0.5 oz bottles, Mfg
Hazard: Lack of Assurance of Sterility
April 15, 2026DrugsFDA
Fagron Compounding Services recalls Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wi
Hazard: Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
April 15, 2026DrugsFDA
Fagron Compounding Services recalls Vancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N.
Hazard: Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
April 15, 2026DrugsFDA
Fagron Compounding Services recalls Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N
Hazard: Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port