FDA•LOW
Pred Mild Ophthalmic Suspension
AbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.
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FDA•LOWLidocaine HCl Injection 2%Eugia US LLC is recalling Lidocaine HCl Injection 2% single-dose vials because the label wrap obscures the barcode, preventing it from scanning.
FDA•LOWNicotine Transdermal System Patch 14 mgAveva is recalling 14 mg Nicotine Transdermal System Patches due to elevated levels of oxidative-related impurities.
FDA•LOWBusulfan InjectionSagent Pharmaceuticals is recalling Busulfan Injection (NDC 25021-241-10) due to failed impurities and degradation specifications.
FDA•LOWPrimidone Tablets 250 mgAmerican Health Packaging is recalling Primidone Tablets 250 mg due to cross-contamination with trace amounts of Acemetacin.
2 products
FDA•LOWPrimidone 50 mg TabletsGolden State Medical Supply is recalling Primidone 50 mg Tablets (NDC 51407-637-05) due to potential cross-contamination with Acemetacin.
2 products- FDA•LOWPrimidone 250mg Tablets
Lannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.
CPSC•LOWLil Pick Up Rex110 and Sierra110 Youth ATVsLil Pick Up recalls 4,900 Rex110 and Sierra110 youth ATVs over crash hazard, suspension defects, and burn risk from hot footwell surfaces.
FDA•LOWLevocarnitine Injection, USP 1 g/5 mLAmerican Regent is recalling Levocarnitine Injection 1 g/5 mL vials (NDC 0517-1045-01) due to missing label.
CPSC•LOWCasely Power Banks 5000mAh MagSafe Wireless ChargerCasely recalls 5000mAh Power Banks (model E33A) over lithium-ion battery fire risk; one fatality reported.
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•LOWBuspirone Hydrochloride Tablets 5 mgUnichem is recalling 500-count bottles of Buspirone Hydrochloride Tablets, 5 mg, due to subpotency.
FDA•LOWCVS Lidocaine Wound GelCVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
FDA•LOWAmprol 25% Medicated ArticleHuvepharma is recalling one bag of Amprol 25% medicated article due to missing lot number and expiration date information.
FDA•LOWMagnesium Chloride 6-Hydrate Crystal 500GAvantor is recalling Magnesium Chloride 6-Hydrate Crystal 500G bottles (NDC 10106-2448-1) due to subpotency.
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•LOWHeraeus PALAMIX uno Mixing SystemHeraeus is reducing the shelf life of the PALAMIX uno mixing system to 17 months due to a potential mixing rod detachment issue.
2 products
FDA•LOWGarland Fresh Peeled GarlicGarland Fresh Peeled Garlic 6 oz. bags are recalled due to potential Clostridium botulinum contamination.
2 products
FDA•LOWSunRidge Farms Organic Black BeansSunRidge Farms Organic Black Beans are being recalled due to potential contamination with haloxyfop and thiamethoxam pesticides.
3 products
FDA•LOWBee Well Wildflower HoneyBee Well Honey is recalling three sizes of Wildflower Honey due to high C4 sugar content, indicating the product may not be 100% pure.
FDA•LOWRemedy Gel Hydrocortisone 1%Island Kinetics is recalling Remedy Gel hydrocortisone 1% due to subpotency.
3 products
FDA•LOWPopping Boba RTD Mixed Berry Hibiscus TeaPocas International is recalling Popping Boba RTD Mixed Berry Hibiscus Tea due to a packaging integrity issue.
4 products
FDA•LOWYunker Energy & Health Herbal SupplementSato Pharmaceutical is recalling Yunker Energy & Health Herbal Supplement because it does not meet label claims for Vitamin E content.
CPSC•LOWWeber Metal Wire Bristle Grill BrushesWeber is recalling 3.2M metal wire bristle grill brushes (models 6277–6494) due to detachable bristles posing ingestion and internal injury risk.
FDA•LOWC2O Coconut Water with PulpC2O Coconut Water with Pulp is recalled due to an incorrect ingredient label on the outer box that omits added sugar content.
FDA•LOWMei Heong Yuen Tangerine Flavor Roasted PeanutsMei Heong Yuen Tangerine Flavor Roasted Peanuts are recalled due to the presence of cyclamates, an unapproved sweetener.
3 products
FDA•LOWGelatin Capsule Pack for Sodium Iodide I-131 KitInternational Isotopes recalling Gelatin Capsule Packs (NDC 69208-003-15/25/35) for Sodium Iodide I-131 Kit due to failed specifications.
FDA•LOWNilotinib Capsules 150 mgCipla is recalling Nilotinib Capsules 150 mg due to failed stability specifications observed during long-term testing.
2 products
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.
- Device RecallFDA•LOWCardiosave Battery Charging Station
Datascope is recalling Cardiosave Battery Charging Stations due to a screw defect in the left bay that prevents proper battery 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•LOWDoxazosin Tablets, USP 4 mgUnichem is recalling Doxazosin Tablets 4 mg (NDC 29300-353-10) due to incorrect tablet imprinting that may cause medication errors.
FDA•LOWLubna Quality Products Mung BeansLubna Quality Products is recalling 4 lb mung bean packages due to unapproved pesticide (Thiamethoxam) contamination.
FDA•LOWSodexo Stars Saccharin Pink PacketsSodexo Stars Saccharin (Pink) packets are recalled due to undeclared aspartame, which may pose a risk to individuals with PKU.
FDA•LOWStraumann WB Impression Post Closed TrayStraumann is recalling WB Impression Post Closed Tray kits (L 13mm) due to incorrect magenta impression caps instead of brown.