FDA•LOW
Povidone Iodine/Proparacaine Ophthalmic Solution
Imprimis NJOF recalls ophthalmic solution for being subpotent, risking reduced efficacy.
Filters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
FDA•LOWFluphenazine HCl Tablets 1mgAjanta Pharma recalls Fluphenazine HCl 1mg tablets (NDC 27241-255-01) due to impurity out-of-specification.
FDA•LOWTrokendi XR (topiramate) Extended-Release CapsulesTrokendi XR (topiramate) 50 mg capsules recalled over failed dissolution specs.
FDA•LOWWonton Specialists: 6 productsWonton Specialist recalls noodles and dumpling skins for undeclared FD&C Red No. 40, an allergen risk.
6 products
FDA•LOWApheresis Red Blood Cells, Leukocytes Reduced, IrradiatedNew York Blood Center recalls apheresis red blood cells over incorrect anticoagulant ratio.
FDA•LOWDoxylamine Succinate and Pyridoxine HCl Delayed-Release TabletsBionpharma recalls Doxylamine Succinate and Pyridoxine HCl 10 mg/10 mg tablets over foreign tablets or capsules.
FDA•LOWAfricando Alfredo Hot SauceAfricando Alfredo Hot Sauce recalled for undeclared wheat and soy allergens.
FDA•LOWIbuprofen Oral Suspension SyringesSafecor recalls Ibuprofen oral suspension syringes over cross-contamination risk.
FDA•LOWParagon 28 Navicular Cage Foot ImplantParagon 28 recalls Navicular Cage foot implant (Model 6123S R) due to elevated oxygen levels.
2 products
FDA•LOWHoneyville Yellow Color 1 GallonHoneyville Yellow Color 1-gal recalled for undeclared Red #40 allergen.
FDA•LOWKanni Delight Fresh Frozen Vannamei White ShrimpKanni Delight Fresh Frozen Vannamei White Shrimp recalled over nitrofurans detected in the product.
FDA•LOWPediatric PN TPN BagsCentral Admixture recalls pediatric TPN bags due to incorrect formulation.
FDA•LOWApheresis PlateletsRed Cross recalls Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced units lacking required yield testing.
FDA•LOWSyva Emit Tox Tricyclic Antidepressant Calibrator/ControlsSiemens recalls Syva Emit Tox Tricyclic Antidepressant Calibrator/Controls due to out-of-specification sodium azide concentration.
FDA•LOWSyva Emit Disopyramide AssaySiemens recalls Syva Emit Disopyramide Assay due to out-of-spec sodium azide concentration; risk of mild irritation.
FDA•LOWAscend Laboratories: Multiple Dabigatran Etexilate CapsulesAscend recalls Dabigatran Etexilate 75mg/150mg capsules over impurity spec failures.
6 products
FDA•LOWShandong Ling Xian Food: 6 Serve Hot Or Cold IngredientsIsland Pacific and Nautilus imitation crab sticks and flakes recalled for undeclared STTP.
6 products
FDA•LOWLidolog KitLidolog Kit is being recalled because the label wrap obscures the barcode, making it difficult to scan.
2 products
FDA•LOWTrokendi XR Topiramate ER Capsules 25mgSupernus recalls Trokendi XR 25mg capsules over failed dissolution specs.
3 products- FDA•LOWAscend Laboratories: Multiple Dabigatran Etexilate Capsules
Ascend recalls Dabigatran etexilate capsules (110 mg, 150 mg) over impurity test failures.
2 products 
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•LOWLunch Box Kitchen Turkey & Cheddar SubLunch Box Kitchen Turkey & Cheddar Sub recall: mislabeled (may be roast beef & Swiss); BEST BY 06/14/26.
FDA•LOWUnited Salt Corp SaltUnited Salt Corp recalls mislabeled salt: plain vs. iodized mix-up.
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 Milk 3 ozMothers' Milk Bank of Louisiana recalls 3 oz Pasteurized Donor Human Milk over potential physical contamination.
FDA•LOWEstrella Passion Fruit DrinkEstrella is recalling its Passion Fruit Drink due to undeclared FD&C Red 40.
FDA•LOWWeikfield Custard Powder Kesar PistaWeikfield recalls Kesar Pista Custard Powder 300g over mislabeled ingredient (Pista vs. 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•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 Tablets 250 mg due to trace Acemetacin 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 mgPrimidone 50 mg tablets recalled due to possible cross-contamination with Acemetacin.
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•LOWCVS Lidocaine Wound GelCVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
FDA•LOWPALAMIX uno Mixing UnitHeraeus recalls PALAMIX uno mixing units: mixing rod may loosen in units over 17 months old; shelf life reduced to 1.5 years.
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.
CPSC•LOWLil Pick Up Youth ATVsLil Pick Up is recalling Rex110 and Sierra110 youth ATVs due to crash and burn hazards that pose a risk of serious injury or death.
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.
CPSC•LOWCasely Power Pods Wireless Power BanksCasely is recalling 5000mAh Power Pods wireless chargers due to fire and burn hazards that have caused serious injuries and one fatality.
FDA•LOWBee Well Wildflower HoneyBee Well is recalling Wildflower Honey in 12, 22, and 44 oz jars over high C4 sugar content.
FDA•LOWIsland Kinetics: multiple gelsIsland Kinetics recalls hydrocortisone 1% gels (Remedy Gel, Skin Rehab, Essential Calming) 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.