All recalls
99,768 total · page 6/3326
- 2026-04-15FDA-DeviceSiemens Medical Solutions USA, IncClass IIARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.
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.
- 2026-04-15FDA-FoodAYCO FARMS INCClass IFresh Cantaloupe (Whole, Fresh), brand name Ayco, wrapped in food safe plastic bags packed in corrugated cardboard cartons; 6-12 melons per box; individual carton count per label. Keep refrigerated; store between 36 40¿F.
Potential Salmonella Contamination
- 2026-04-15FDA-FoodBlueroot Health, Inc.Class IIVital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count bottles
Contains undeclared egg, soy, and hazelnut
- 2026-04-15FDA-FoodRiverence Provisions LLCClass IIRiverence Smoked Trout Dip, net wt. 7oz. Product is perishable, refrigerated, packaged in plastic tub. Product is shipped to consignee frozen by the case (12/7oz. units per case). Retail container UPC 7 07651 30561 3. Case item UPC #007076513057 Label declares Ingredients: Smoked Trout, Whipped Cream Cheese, Sour Cream, Horseradish, Lemon Juice, Dill, Black Pepper. Contains: Fish (Rainbow Trout).
Label declares cream cheese but does not declare milk
- 2026-04-15FDA-FoodF&S Fresh Foods, Inc.Class IIReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, perishable, Keep Refrigerated, plastic clamshell, net wt. 10 oz, UPC 8 26766 25036 3. Distributed By F&S Fresh Foods Vineland, NJ 08360. Label declares CONTAINS EGG, MILK, SOY, WHEAT.
Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.
- 2026-04-15FDA-FoodMEI YU CHENG DA TRADING INCClass IIIOlive Skewers individually wrapped and packaged in clear plastic bag; 500g; INGREDIENTS: Olive, edible salt, white sugar, monosodium glutamate, licorice, cloves, food additives (citric acid, DL malic acid, saccharin, sodium saccharin, steviol glycosides, aspartame, vanillin, ethyl malt powder, lemon yellow, carmine, sodium benzoate, potassium sorbate, sodium metabisulfite); MANUFACTURER: Fuzhou Hangzhengiou food Co. Ltd; UPC: 6 922279 985205
Products contain banned sweetener: cyclamates.
- 2026-04-15FDA-FoodMEI YU CHENG DA TRADING INCClass IIIDADI NONGFU DRIED SALT CHILLI VEGETABLE(S); Ingredients: Radish, chili, roasted sesame, prickly ash, edible salt, soybean oil, edible vinegar, white granulated sugar, spices, food additives (sodium glutamate, citric acid, sodium benzoate, potassium sorbate, sodium saccharin, acesulfame, sucralose, disodium EDTA, turmeric).; Allergen: This product contains sesame and soy products; Net Wt. 14.1 oz(400g)
Products contain banned sweetener: cyclamates.
- 2026-04-15FDA-FoodConnecticut Crab Company LLCClass IICrab Cakes various sizes sold to food service
May be temperature abused, which may result in growth of Clostridium botulinum
- 2026-04-15FDA-FoodPure Vitamins and Natural Supplements, LLCClass IRed Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Red Bull Corporation. Turkey www.redbullhoney.com UPC Code 9554100205595
FDA analysis revealed the presence of undeclared sildenafil
- 2026-04-15FDA-FoodPure Vitamins and Natural Supplements, LLCClass IBlue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Blue Bull Corporation Made In USA. UPC Code 707443349917
FDA analysis revealed the presence of undeclared sildenafil
- 2026-04-15FDA-FoodPure Vitamins and Natural Supplements, LLCClass IBoner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume 1 entire pouch 30 minutes before Intercourse. MANUFACTURED IN: FLORIDA. UPC 788362191603
FDA analysis revealed the presence of undeclared sildenafil and Tadalafil
- 2026-04-15FDA-FoodZarlengo Italian IceClass IIZarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper resistant lid.
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- 2026-04-15FDA-FoodZarlengo Italian IceClass IIZarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl oz cups and 32 fl oz cups translucent freezer grade and round High-Density Polyethylene container with lid and 1 Gallon bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper r
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- 2026-04-15FDA-FoodZarlengo Italian IceClass IIZarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon bucket/pail and 2-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl oz cups and 32 fl oz cups translucent freezer grade and round High-Density Polyethylene container with lid and 1-Gallon and 2-Gallon bucket/pail - white round food and freezer grade H
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- 2026-04-15FDA-DrugTeva Pharmaceuticals USA, IncClass IIClonidine Transdermal System, USP, 0.3 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only, Manufactured by: Actavis Laboratories UT Inc., Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc, Parsippany, NJ, NDC 0591-3510-04 carton, NDC 0591-3510-54 pouch
CGMP Deviations: use of an unapproved raw material
- 2026-04-15FDA-DrugTeva Pharmaceuticals USA, IncClass IIClonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only, Manufactured by: Actavis Laboratories UT Inc., Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc, Parsippany, NJ, NDC 0591-3509-04 carton, NDC 0591-3509-54 pouch
CGMP Deviations: use of an unapproved raw material
- 2026-04-15FDA-DrugTeva Pharmaceuticals USA, IncClass IIClonidine Transdermal System, USP, 0.1 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx Only, Manufactured by: Actavis Laboratories UT Inc., Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc, Parsippany, NJ, NDC 0591-3508-04 carton, NDC 0591-3508-54 pouch
CGMP Deviations: use of an unapproved raw material
- 2026-04-15FDA-DrugGE Healthcare Ireland LimitedClass IIGE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1414-91.
Presence of particulate matter
- 2026-04-15FDA-DrugGE Healthcare Ireland LimitedClass IIGE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1413-63.
Presence of particulate matter
- 2026-04-15FDA-DrugTeva Pharmaceuticals USA, IncClass IIIsotretinoin Capsules, USP, 40 mg, 10 count Prescription Pacs, Rx only, Manufactured for: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0591-2436-15 (carton), NDC 0591-2436-45 (blister pack).
Superpotent and Subpotent
- 2026-04-15FDA-DrugTeva Pharmaceuticals USA, IncClass IIIsotretinoin Capsules, USP, 30 mg, Rx Only, 10 count Prescription Pack, Manufactured for: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0591-2435-15 (carton), NDC 0591-2435-45 (blister pack).
Superpotent and Subpotent
- 2026-04-15FDA-DrugViatris, Inc.Class IIXanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty LLC, Morgantown, WV 06506, U.S.A, Made in Ireland, NDC 58151-506-91
Failed Dissolution Specifications
- 2026-04-15FDA-DrugPreferred Pharmaceuticals, Inc.Class IIArtificial Tears Lubricant Eye Drops (glycerin 0.2%, hypromellose 0.2%, polyethylene glycol 400 1%), 0.5 oz bottles, Mfg: Geri-Care; Brooklyn, New York NDC 68788-7266-0
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IIVancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5082-01
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IIVancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5085-01
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IIVancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5083-01
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IInorepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5027-02
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IInorepinephrine Bitartrate,16mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5026-02
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II5% Dextrose Injection, USP 12.5 g per 250 mL (50 mg per mL) 250 mL in a 250 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-458-05, Unit of Sale NDC Number: 65219-458-30.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II5% Dextrose Injection, USP 5 g per 100 mL (50 mg per mL) 100 mL in a 100 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-464-05, Unit of Sale NDC Number: 65219-464-50.
Lack of Assurance of Sterility