FDA•MODERATE
Philips Brilliance iCT Gantry Rotor Fasteners
Philips is recalling Brilliance iCT systems due to a risk of rotor parts becoming unsecured and potentially expelled during gantry rotation.
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FDA•MODERATEOlympus Single Use 3-Lumen Sphincterotome VOlympus is recalling the Single Use 3-Lumen Sphincterotome V (Model KD-V411M-1520) due to a risk of deformation and performance loss.
30 products
FDA•MODERATEMaquet Venous Bubble SensorMaquet is recalling the Venous Bubble Sensor (Model 701055720) due to cable durability issues that may cause device errors.
FDA•MODERATEFDR Visionary Suite X-ray GeneratorFUJIFILM is recalling FDR Visionary Suite X-ray generators due to a risk of overheating and smoke caused by faulty electromagnetic contactors.
FDA•MODERATEBeacon Promotions: 3 productsBeacon Promotions recalls repackaged M&Ms candies due to undeclared milk, soy, and peanut allergens.
3 products
FDA•CRITICALPrime Food Processing Dried Croaker FishPrime Food Processing is recalling 8 oz packages of Dried Croaker Fish due to the risk of Clostridium botulinum toxin 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