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Proin ER Tablets
Pegasus recalls Proin ER 145mg tablets for dogs due to failed dissolution specs.
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FDA•Ascend Laboratories: Multiple Dabigatran Etexilate CapsulesAscend recalls Dabigatran Etexilate Capsules (150 mg, 75 mg) over impurity/degradation failures.
3 products
FDA•Mycophenolate Mofetil for InjectionMylan recalls Mycophenolate Mofetil for Injection 500 mg vials due to precipitate.
FDA•Glycopyrrolate Oral SolutionPrecision Dose recalls Glycopyrrolate Oral Solution over an unidentified impurity.
FDA•Cetirizine Hydrochloride Tablets 5 mgRising Pharma recalls Cetirizine HCl 5 mg tablets over Ranitidine cross-contamination.
FDA•LOWShandong Ling Xian Food Co: 3 productsShandong Ling Xian Food is recalling three imitation crab products due to undeclared sodium tripolyphosphate.
3 products
FDA•LOWLidolog KitLidolog Kit is being recalled because the label wrap obscures the barcode, making it difficult to scan.
FDA•Trokendi XR 25mg CapsulesSupernus Pharmaceuticals is recalling Trokendi XR 25mg capsules due to failed dissolution specifications.
- FDA•Ascend Laboratories: Multiple Dabigatran Etexilate Capsules
Ascend Laboratories is recalling 110 mg and 150 mg Dabigatran etexilate capsules due to failed impurity and degradation specifications.
2 products 
FDA•Divalproex Sodium Delayed-Release TabletsBionpharma is recalling 500 mg Divalproex Sodium Delayed-Release Tablets due to the presence of foreign tablets or capsules in the bottles.
FDA•LOWFexofenadine Hydrochloride Tablets 180 mgOhm Laboratories is recalling 180 mg Fexofenadine Hydrochloride tablets due to failed impurities and degradation specifications.
FDA•LOWHydroxyzine Hydrochloride Oral SolutionANI Pharmaceuticals is recalling Hydroxyzine Hydrochloride Oral Solution, 10 mg/5 mL, due to the presence of a foreign substance.
FDA•LOWRoast Beef and Cheddar Closed Face SandwichProduce Innovations recalls Roast Beef and Cheddar sandwiches mislabeled as Turkey and Cheddar subs, Best By 06/14/26, Lot 26 134.
FDA•LOWUnited Salt SaltUnited Salt recalls salt products due to mislabeling of iodized and plain varieties.
FDA•LOWFocalin XR 5 mg CapsulesSandoz is recalling Focalin XR 5 mg capsules due to missing or incorrect lot numbers and expiration dates on the product labels.
FDA•LOWPrimidone 50 mg TabletsAmneal Pharmaceuticals is recalling Primidone 50 mg tablets due to potential cross-contamination with Acemetacin API.
FDA•LOWPasteurized Donor Human MilkMothers' Milk Bank of Louisiana recalls donor human milk due to a dark spot on the container bottom.
FDA•LOWEstrella Passion Fruit DrinkRefresqueria Estrella is recalling Passion Fruit Drink in 14 oz, 64 oz, and 120 oz bottles due to undeclared FD&C Red 40.
FDA•LOWWeikfield Custard Powder Kesar PistaWeikfield Custard Powder Kesar Pista 300g recalled over mislabeled ingredient (Pista should be Pistachio).
FDA•LOWEpinephrine Injection 1mg/mLFresenius Kabi is recalling Epinephrine Injection 1mg/mL vials due to out-of-specification stability test results.
FDA•LOWYunker Energy & Health Herbal SupplementSato Pharmaceutical is recalling Yunker Energy & Health Herbal Supplement due to a failure to meet label claims for Vitamin E content.
FDA•Udder Products Yeast BlendNutra Blend is recalling 50 lb bags of Udder Products Yeast Blend due to elevated selenium levels.
FDA•LOWLidocaine HCl Injection 2%Eugia US LLC is recalling Lidocaine HCl Injection 2% because the label wrap covers the barcode, making it difficult to scan.
FDA•LOWPred Mild Ophthalmic SuspensionAbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.
FDA•LOWNicotine Transdermal System Patch 14 mgAveva is recalling 14 mg Nicotine Transdermal System Patches due to elevated levels of oxidative-related impurities.
FDA•LOWPrimidone Tablets 250 mgAmerican Health Packaging recalls Primidone 250 mg tablets over API cross contamination.
2 products
FDA•LOWBusulfan InjectionSagent Pharmaceuticals is recalling Busulfan Injection (NDC 25021-241-10) due to failed impurities and degradation specifications.
FDA•LOWPrimidone Tablets 50 mgGolden State Medical Supply is recalling Primidone Tablets 50 mg due to cross-contamination with trace amounts of Acemetacin API.
2 products
FDA•LOWPrimidone 250mg TabletsLannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.
FDA•LOWBuspirone Hydrochloride TabletsUnichem is recalling 5 mg buspirone hydrochloride tablets due to subpotency, which may reduce the medication's effectiveness.
FDA•LOWTops Markets: 2 productsTops Markets recalls Garland Fresh and Christopher Ranch Peeled Garlic 6 oz. bags over botulism risk from temperature abuse.
2 products
FDA•LOWCVS Lidocaine Wound GelCVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
FDA•LOWPALAMIX duo / PALAMIX unoHeraeus recalls PALAMIX duo and uno mixing units due to risk of mixing rod loosening in units over 17 months old.
2 products
FDA•LOWLevocarnitine Injection, USPAmerican Regent is recalling Levocarnitine Injection, USP, 1 g/5 mL single-dose vials due to missing labels.
FDA•LOWMonsel's Ferric Subsulfate Solution 8 mLPremier Dental Products is recalling Monsel's Ferric Subsulfate Solution 8 mL vials (NDC 48783-112-08) due to incorrect expiration date on the vial label.
FDA•LOWMagnesium Chloride 6-Hydrate Crystal 500GAvantor is recalling Magnesium Chloride 6-Hydrate Crystal 500G bottles (NDC 10106-2448-1) due to subpotency.
FDA•LOWAmprol 25% Medicated ArticleHuvepharma is recalling one bag of Amprol 25% medicated article due to missing lot number and expiration date information.
FDA•LOWBee Well Wildflower HoneyBee Well Honey is recalling Wildflower Honey due to high C4 sugar content, indicating the product is not 100% pure.
FDA•LOWIsland Kinetics: multiple drugsIsland Kinetics recalls three hydrocortisone 1% gels due to subpotency.
3 products
FDA•LOWFarmina Pet Foods N&D Tropical Selection Dog FoodFarmina Pet Foods N&D Tropical Selection dog food (22 lb, UPC 8 01027 60423 85) recalled due to mislabeling—front lists salmon, back lists lamb.
FDA•LOWPocas International: 4 productsPocas International recalls four Popping Boba RTD teas in 13.8 oz cans over packaging integrity issues.
4 products- Food RecallFDA•LOWSuper World Trading: 3 products
Super World Trading recalls Mei Heong Yuen roasted peanuts due to banned cyclamate sweetener.
3 products 
FDA•LOWFalcon Trading Co: 3 productsFalcon Trading recalls SunRidge Farms organic beans and soup mix over pesticide contamination.
3 products
FDA•LOWSodium Iodide I-131 Kit Gelatin Capsule PackRadnostix is recalling Sodium Iodide I-131 Kit capsule packs due to failed product specifications.
FDA•LOWDatascope Cardiosave Battery Charging StationDatascope is recalling the Cardiosave battery charging station due to a screw defect in the left bay that prevents proper charging.
FDA•LOWPitavastatin Tablets, 2 mgNorthstar Rx LLC is recalling Pitavastatin Tablets, 2 mg (NDC 72603-479-01) due to a foreign 1 mg tablet found in bottles.
FDA•LOWC2O Coconut Water with PulpC2O Coconut Water with Pulp is recalled due to incorrect nutrition labeling on the outer cardboard box that omits added sugar content.
FDA•LOWCipla: Multiple Packaged In Cartons CapsulesCipla recalls Nilotinib Capsules (150 mg, 200 mg) over failed stability tests for appearance.
2 products
FDA•LOWLubna Quality Products Mung BeansLubna Quality Products is recalling 4 lb mung bean packages due to unapproved pesticide (Thiamethoxam) contamination.
FDA•LOWEptifibatide Injection 75 mg/100 mLSlate Run Pharmaceuticals recalls Eptifibatide Injection 75 mg/100 mL vials (NDC 70436-027-80, 70436-163-80) due to incorrect dosing-route labeling.