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Kitchen HQ Thermal Insulated Bowls
Kitchen HQ thermal insulated bowls are being recalled due to a fire hazard when used in a microwave.
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CPSC•Sloosh Dive SticksJoyin is recalling Sloosh dive sticks (model 40041) due to an impalement hazard that violates the federal dive sticks ban.
CPSC•Kawasaki Teryx4 H2 and Teryx5 H2 Off-Road VehiclesKawasaki is recalling 2026 Teryx4 H2 and Teryx5 H2 off-road vehicles due to a drive converter sheave failure that poses impact and injury risks.
CPSC•LiKee Pull String Teething ToysLiKee Pull String teething toys (Model LK-FDWJ) are recalled due to a choking hazard that violates federal toy safety standards.
CPSC•Merkury Innovations Hot + Cool FansMerkury Innovations is recalling model MI-DHC02 Hot + Cool fans due to an overheating fire hazard that poses a risk of serious injury or death.
CPSC•Nimood Adult Portable Bed RailsNimood is recalling C3 Pro, C4 Pro, C5 Pro, and C5 Pro 2.0 adult portable bed rails due to serious entrapment and asphyxiation hazards.
CPSC•Childcraft Furniture Tip Restraint KitsSchool Specialty is recalling tip restraint kits included with Childcraft furniture due to tip-over and entrapment hazards.
CPSC•Timechee Changing Table DressersTimechee changing table dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.
CPSC•Yamaha Drive2 Electric Fleet Golf CarsYamaha is recalling 2021-2022 Drive2 Electric Fleet Golf Cars due to a brake cable defect that poses a crash and injury risk.
CPSC•Yamaha UMAX Bistro and Bistro Deluxe VehiclesYamaha is recalling 2019–2025 UMAX Bistro and Bistro Deluxe vehicles due to an inaccurate weight capacity label that poses an injury hazard.
FDA•CRITICALAzuma Foods Tako Wasabi Seasoned OctopusAzuma Foods is recalling Tako Wasabi Seasoned Octopus due to undeclared fish.
FDA•MODERATENiacin Extended-Release Tablets 1,000 mgGolden State Medical Supply is recalling Niacin Extended-Release Tablets, 1,000 mg, due to failure to meet dissolution specifications.
2 products
FDA•MODERATEFresh Roast Systems ColorTrack InstrumentFresh Roast Systems is recalling the ColorTrack instrument (Model BENCH R-100) due to a potential laser safety hazard.
FDA•MODERATEHalyard Pain PackAVID Medical recalls Halyard Pain Pack kits (AMPK48-01) over possible lack of sterilization.
4 products
FDA•MODERATEMOSAIQ Oncology Information SystemElekta is recalling the MOSAIQ Oncology Information System due to a software error that may prevent the loading of baseline shift plans.
FDA•MODERATEBoston Scientific Orca Air/Water and Suction ValvesBoston Scientific is recalling Orca single-use air/water and suction valves due to reports of the suction button sticking during use.
- Device RecallFDA•MODERATEMerlin Patient Care System Programmer Software
Abbott Medical is recalling Merlin PCS software for the Model 3330 programmer due to a potential failure to terminate pacing tests.
FDA•MODERATEBoston Scientific Clik X AnchorBoston Scientific is recalling the Clik X Anchor due to a potential lack of sterility assurance.
FDA•MODERATEBoston Scientific CSK ElectrodesBoston Scientific recalls CSK reusable electrodes over performance concerns.
4 products
FDA•MODERATEBicarby DialysateFresenius Medical Care is recalling Bicarby Dialysate due to a GTIN labeling error that may result in the use of an incorrect potassium solution.
FDA•LOWPrimidone 50 mg TabletsAmneal Pharmaceuticals is recalling Primidone 50 mg tablets due to potential cross-contamination with Acemetacin API.
FDA•MODERATEMinocycline Hydrochloride 115 mg TabletsAscend Laboratories is recalling Minocycline Hydrochloride 115 mg tablets due to failed dissolution specifications.
FDA•MODERATENeuro Nourish Dietary SupplementSensory Supplement is recalling Neuro Nourish dietary supplement due to premature lipid oxidation causing off odors and bitter taste.
3 products
FDA•MODERATEZep Alcohol Sanitizer SprayZep Inc. is recalling 55-gallon containers of Alcohol Sanitizer Spray due to potential microbial contamination.
FDA•MODERATEAdvance Aluminum Chloride Gel Hemostatic KitInter-Med is recalling Aluminum Chloride Gel kits due to an incorrect package insert that provides dangerous first aid instructions.
FDA•MODERATEDragonfly Thai Ginger PowderDragonfly Thai Ginger Powder is being recalled due to potential lead contamination.
FDA•MODERATEHintermann Series Talar ImplantDT MedTech is recalling the Hintermann Series Talar Implant due to a labeling error that may result in the wrong implant being used.
FDA•MODERATESiemens Dimension Tacrolimus Flex Reagent CartridgeSiemens is recalling Dimension Tacrolimus Flex reagent cartridges due to a potential positive bias in test results.
FDA•MODERATEPark St. Deli Macaroni & CheesePark St. Deli Macaroni & Cheese is recalled due to an undeclared soy lecithin allergen.
FDA•CRITICALClover Hill Dairy LLP: 18 productsClover Hill Dairy recalls multiple soft cheeses (Ricotta, Cuajada, Cheddar) over Listeria risk. Discard or return.
18 products
FDA•LOWPasteurized Donor Human Milk 3 ozMothers' Milk Bank of Louisiana recalls 3 oz Pasteurized Donor Human Milk over potential physical contamination.
FDA•CRITICALBeekeeper's Naturals Saline Nasal SprayBeekeeper's Naturals recalls Saline Nasal Spray due to microbial contamination.
2 products
FDA•LOWEstrella Passion Fruit DrinkEstrella is recalling its Passion Fruit Drink due to undeclared FD&C Red 40.
FDA•MODERATEFarm Rich Pizza Cheese CrunchersFarm Rich Pizza Cheese Crunchers recalled over possible metal pieces.
FDA•MODERATEMedartis APTUS Cannulated Compression ScrewsMedartis is recalling APTUS cannulated compression screws due to a manufacturing defect where the cannulation is not centered.
FDA•MODERATEEXENT AnalyserThe Binding Site is recalling the EXENT Analyser due to a software error that may cause inaccurate M-protein detection or measurements.
FDA•MODERATEGalaxy RG: 23 One Unit Per ContainersGalaxy RG recalls Brazo Gitano and other bakery items over undeclared Yellow #5, Yellow #6, and Red #40.
23 products
FDA•CRITICALSteve's Real Food Chicken Recipe Freeze DriedSteve's Real Food is recalling 1.25 lb bags of Chicken Recipe Freeze Dried cat food due to inadequate thiamine levels.
FDA•MODERATEBudesonide Inhalation SuspensionSun Pharmaceutical is recalling Budesonide Inhalation Suspension (1mg/2mL) due to the presence of foreign black or brown particles.
FDA•MODERATEBreckenridge Pharmaceutical: multiple capsulesBreckenridge recalls Duloxetine 30mg and 60mg capsules due to N-nitroso-duloxetine impurity above FDA limit.
2 products
FDA•MODERATENeoSpan SuperElastic Compression StapleIn2bones USA is recalling 10+ variants of NeoSpan compression staples due to missing MR Conditional safety labeling.
2 products
FDA•LOWWeikfield Custard Powder Kesar PistaWeikfield recalls Kesar Pista Custard Powder 300g over mislabeled ingredient (Pista vs. Pistachio).
FDA•CRITICALCareFusion 213: Multiple Chlorhexidine Gluconate SolutionsBD recalls ChloraPrep Clear and FREPP Clear applicators due to sterility seal breach risk.
4 products
FDA•MODERATECareFusion 213: Multiple Subsidiary Of Beckton SolutionsBD recalls ChloraPrep & PurPrep applicators due to lack of sterility assurance, posing infection risk.
10 products
FDA•CRITICALRequeson (Soft Ricotta) 1 lbNelson & Isa Lacteos recalls Requeson (soft ricotta) 1 lb over possible Listeria contamination.
FDA•LOWEpinephrine Injection 1mg/mLFresenius Kabi is recalling Epinephrine Injection 1mg/mL vials due to out-of-specification stability test results.
FDA•MODERATEPhilips DigitalDiagnost C90 Wall StandPhilips is recalling DigitalDiagnost C90 systems because the Wall Stand VS2 lacks a required seismic stability kit.
FDA•MODERATEMicromed SD LTM 64 PLUS EEG AmplifierMicromed is recalling SD LTM 64 PLUS EEG amplifiers due to a potential one-second temporal delay that may cause misinterpretation of results.
FDA•MODERATECGuard Prime Carotid Stent SystemInspireMD recalls CGuard Prime Carotid Stent System (model CND0830) due to deployment complications.
6 products
FDA•MODERATECORFLO Safety PEG KitAvanos recalls CORFLO Safety PEG Kit (model 30-4320) due to supplier-recalled lidocaine.
20 products