FDA•CRITICAL
Made Fresh Salads: 14 Brand Tubs
Made Fresh Salads recalls 14 varieties of 5 lb whipped cream cheese over possible Listeria contamination.
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FDA•MODERATEGerber Arrowroot BiscuitsGerber Arrowroot Biscuits (5.5 oz, UPC 015000005962) recalled for potential paper/plastic contamination in arrowroot flour.
FDA•MODERATEHitachi Proton Beam Therapy SystemHitachi recalls Proton Beam Therapy System over patient positioning software anomaly.
2 products- Food RecallFDA•MODERATEKeto-C Antiseptic Wipes
Stratford Care USA is recalling Keto-C Antiseptic Wipes (50ct) due to misbranding; product contains non-medicated otic flush instead of labeled antiseptic.
36 products 
FDA•MODERATESpicy Breakfast Burrito 10 ozMG Foods recalls Spicy Breakfast Burrito 10 oz over possible plastic fragments.
FDA•MODERATETKS Co-pack Manufacturing: 2 productsAonic recalls His & Hers supplement shots over possible E. coli and coliform contamination.
2 products
FDA•MODERATEFrozen Cooked Medium ShrimpH & N Group is recalling 1 lb bags of frozen cooked medium shrimp due to potential Cesium-137 contamination.
FDA•MODERATEMcCain Foods: 2 productsMcCain Foods recalls Ore-Ida Tater Tots and Sonic Tots over possible small hard plastic fragments.
2 products
FDA•MODERATERed Button Movie House PopcornRed Button Movie House Popcorn is being recalled due to the potential presence of foreign material.
FDA•LOWSodexo Stars Saccharin PacketsDomino Foods recalls Sodexo Stars Saccharin Packets due to undeclared aspartame.
FDA•CRITICALKirkland Signature Mini BeignetsKirkland Signature Mini Beignets are recalled due to undeclared hazelnut, which poses a risk to consumers with allergies.
FDA•CRITICALUdenyca Pegfilgrastim-cbqv InjectionAccord BioPharma is recalling Udenyca injection due to improper storage temperature conditions.
FDA•MODERATEOxycodone Hydrochloride 5 mg TabletsAmerican Health Packaging is recalling Oxycodone 5 mg tablets due to defective blister card seals that may cause tablets to fall out.
FDA•MODERATECetrorelix Acetate Injection KitMeitheal Pharmaceuticals is recalling Cetrorelix Acetate injection kits due to missing or duplicated needles in the delivery system.
FDA•CRITICALOlympus High Flow Insufflation UnitOlympus is recalling the UHI-3 High Flow Insufflation Unit due to a software issue that may cause dangerous overpressure events.
3 products
FDA•MODERATELaerdal Compact Suction Unit 4 RTCALaerdal is recalling LCSU 4 RTCA suction units due to potential electromagnetic noise levels exceeding regulatory limits.
FDA•CRITICALGo Raw: 2 Steves Real Food AumsvillesQuest Cat Food recalled for inadequate thiamine levels; stop feeding and contact Steve's Real Food.
2 products
FDA•MODERATEMedline Surgical and Biopsy Convenience KitsMedline is recalling various surgical and biopsy convenience kits due to potential issues with the sterility assurance level.
62 products
FDA•MODERATEAuris Health MONARCH Platform Bronchoscopy SystemAuris Health is recalling MONARCH Platform Bronchoscopy systems due to a software issue that may cause unexpected robotic arm repositioning and contact with the patient.
FDA•MODERATEMOLLI 2 Surgical Marker SystemStryker is updating the MOLLI 2 System labeling due to the risk of magnetized surgical tools dislodging markers during tissue removal.
2 products
FDA•MODERATETippy Toes Apple Pear Banana Baby FoodTippy Toes Apple Pear Banana baby food is recalled due to potential patulin contamination.
FDA•CRITICALWhite Vein Advanced Alkaloids Chewable TabletsShaman Botanicals recalls White Vein Advanced Alkaloids chewable tablets due to excess 7-hydroxymitragynine.
4 products
FDA•CRITICALRosabella Moringa Dietary Supplement CapsulesAmbrosia Brands is recalling Rosabella Moringa dietary supplement capsules due to potential Salmonella contamination.
FDA•MODERATEThiamine HCl Injection 500 mg/100 mLFresenius Kabi recalls thiamine HCl 500 mg/100 mL IV bags over sterility concerns.
5 products
FDA•MODERATEMediHoney Gel DressingIntegra LifeSciences is recalling MediHoney Gel dressing models 31805 and 31815 due to a potential breach in the sterile packaging barrier.
3 products
FDA•MODERATESpectrum IQ Infusion PumpBaxter is recalling Spectrum IQ Infusion Pumps (Model 3570009) due to incomplete testing of occlusion alarm functionality.
FDA•MODERATECrunchy Caramel Dark Chocolate BarsCacao Art recalls Crunchy Caramel dark chocolate bars (2 oz) for undeclared milk allergen.
FDA•CRITICALJuniper Granola: 4 All Natural Snack BarsJunebar snack bars recalled for undeclared milk and soy allergens.
4 products
FDA•MODERATEWellsley Farms Atlantic Salmon 32 ozWellsley Farms Atlantic Salmon 32 oz recalled over Listeria risk.
FDA•MODERATESmoked Grouper DipIsland Crab recalls Smoked Grouper Dip 7 lb tubs due to undeclared milk, eggs, and sulfites.
FDA•MODERATEGluten Free Seasoned Vegan Pizza CrustRich Products Corp is recalling Gluten Free Seasoned Vegan Pizza Crusts due to undeclared milk and egg allergens.
2 products
FDA•MODERATETestosterone 100 mg Sterile PelletsAsteria Health recalls Testosterone 100 mg Sterile Pellets over possible metal contamination.
25 products
FDA•MODERATEDiclofenac Sodium Topical Gel 3%Taro Pharmaceuticals is recalling Diclofenac Sodium Topical Gel 3% (100 g) due to viscosity specification failure.
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•MODERATETrazodone Hydrochloride 50 mg TabletsGranules Pharmaceuticals is recalling Trazodone Hydrochloride 50 mg tablets (NDC 70010-231-01) due to foreign tablets or capsules in bottles.
- 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•MODERATEWinCo Foods Deli Margherita PizzaWinCo Foods is recalling Deli Margherita Pizza Thin Crust due to potential metal fragment contamination.
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•MODERATEPreema Bright Red and Orange Food Colour PowderPreema Bright Red and Orange Food Colour Powder recalled for banned carmoisine and undeclared FD&C Yellow 5 and Red 40.
2 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•MODERATEFrozen Half Shell OystersKhee Trading is recalling frozen half shell oysters due to potential Norovirus contamination.
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•CRITICALOutside The Breadbox Bread CrumbsOutside The Breadbox Bread Crumbs recalled for undeclared egg and milk allergens.