FDA•MODERATE
Trazodone Hydrochloride 50 mg Tablets
Granules Pharmaceuticals is recalling Trazodone Hydrochloride 50 mg tablets (NDC 70010-231-01) due to foreign tablets or capsules in bottles.
Filters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←- Device RecallFDA•MODERATEPhilips Azurion 5 M20 and 7 M12 Systems
Philips recalls Azurion 5 M20 and 7 M12 systems over risk of unexpected table movement when Reset Geometry is pressed.
8 products 
FDA•MODERATEAlphatec Spine Lateral Navigation Disc Prep InstrumentsAlphatec Spine is recalling 10mm Osteotome navigation instruments due to a design flaw in the array connection geometry.
2 products
FDA•MODERATEPro Numb Tattoo Numbing SprayPro Numb Tattoo Numbing Spray recalled over cGMP deviations.
2 products
FDA•MODERATEHalyard Transport Bag Kit LIFE0080-01Halyard Transport Bag Kit LIFE0080-01 recalled due to Tyvek bag seal issue that may compromise sterility.
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.
FDA•CRITICALTRUE METRIX Blood Glucose Meter InstructionsTrividia recalls TRUE METRIX meter instructions over inadequate E-5 error guidance.
7 products
FDA•MODERATEPhilips Brilliance iCT Gantry Rotor FastenersPhilips is recalling Brilliance iCT systems due to a risk of rotor parts becoming unsecured and potentially expelled during gantry rotation.
4 products
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•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•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•MODERATEEncore Medical EMPOWR Acetabular and Knee InsertsEncore Medical is recalling EMPOWR acetabular liners and knee inserts due to a packaging discrepancy that may cause surgical delays.
2 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•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