FDA•CRITICAL
Outside The Breadbox Bread Crumbs
Outside The Breadbox Bread Crumbs recalled for undeclared egg and milk allergens.
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FDA•MODERATEOrganic Spices: 3 No Artificial Coloring No Gluten CasSpicely organic garlic salt, celery salt, and sumac recalled for mislabeling due to undeclared salt.
3 products
FDA•CRITICALOrganic Black Chia SeedsTradin Organics is recalling 55.12 lb bags of organic black chia seeds due to potential Salmonella contamination.
FDA•MODERATEVITEK 2 Gram-negative Susceptibility CardsBiomerieux is recalling 30+ VITEK 2 susceptibility cards due to potential quality control failures and false resistant test results.
2 products
FDA•MODERATEPrismaflex M100 SetVantive is recalling the Prismaflex M100 Set due to a potential dislodgement of the deaeration chamber from the control unit.
8 products
FDA•MODERATEBisoprolol Fumarate and Hydrochlorothiazide Tablets 2.5 mg/6.25 mgUnichem Pharmaceuticals recalls Bisoprolol/Hydrochlorothiazide 2.5/6.25 mg tablets (NDC 29300-187-01) due to N-Nitroso Bisoprolol impurity specification failure.
FDA•CRITICALWhy Not Natural Moringa CapsulesWhy Not Natural is recalling Moringa Capsules distributed nationwide due to potential Salmonella contamination.
FDA•MODERATEMethylprednisolone Tablets USP Dosepak 4 mgGreenstone is recalling methylprednisolone 4 mg tablets (NDC 59762-4440-2) due to incorrect blister foil orientation causing incorrect dosing information.
FDA•CRITICALNavitas Organics Organic Chia SeedsNavitas Organics recalls Organic Chia Seeds 8 oz over possible Salmonella contamination.
FDA•MODERATEFurosemide Tablets USP 40 mgRising Pharmaceuticals is recalling Furosemide Tablets 40 mg (NDC 64980-563-10) due to foreign substance contamination.
FDA•MODERATEThyroid, USPSpecialty Process Labs is recalling Thyroid, USP (NDC 81305-100-02) due to subpotency.
FDA•CRITICALSUPERFOODS: 4 Live It Up Brand Super GreensLive it Up Super Greens recalled over possible Salmonella Typhimurium contamination.
4 products
FDA•MODERATELanreotide Injection 120 mg/0.5 mLCipla is recalling Lanreotide Injection 120 mg/0.5 mL due to the presence of particulate matter.
FDA•MODERATEAQ 120 GFEW Aquarion Preserved CartridgesEncon Safety Products is recalling AQ 120 GFEW Aquarion Preserved Cartridges due to cGMP manufacturing deviations.
FDA•CRITICALSpring & Mulberry: 11 Retail Product Sold Individually Or AsSpring & Mulberry recalls 11 varieties of Date-Sweetened Chocolate bars over potential Salmonella contamination.
11 products
FDA•MODERATEDiva Fam: 14 Sea Moss Gel SuperfoodsDiva Fam recalls all flavors of Sea Moss Gel Superfood (16 oz) over botulism risk.
14 products
FDA•CRITICALHerbs Forever: 2 Ayruvedic Herbal SupplementsHerbsForever recalls Gastro Care and Hingwastika Churna supplements over undeclared wheat allergen.
2 products