FDA•MODERATE
Soft-Vu Angiographic Catheter
Angiodynamics is recalling Soft-Vu angiographic catheters due to a manufacturing defect that may block the catheter hub.
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FDA•MODERATEChina Noodle Co. Steam NoodlesChina Noodle Co. Steam Noodles are recalled due to undeclared wheat, a potential allergen risk for consumers.
4 products
FDA•MODERATEChildren's Ibuprofen Oral Suspension 100 mg/5mLTaro Pharmaceuticals is recalling Children's Ibuprofen Oral Suspension 100 mg/5mL (120 mL) due to gel-like masses and black particles.
FDA•CRITICALWebcol Alcohol Prep Pads (70% Isopropyl Alcohol)Cardinal Health is recalling Webcol Alcohol Prep Pads (200-count boxes) due to microbial contamination that may pose infection risk.
3 products
FDA•MODERATEeTRAX Needle System Starter KitCivco is recalling the eTRAX Needle System Starter Kit 18G due to a risk of incorrect needle tip positioning on the user interface.
8 products
FDA•CRITICALPhilips Respironics Trilogy Evo VentilatorPhilips Respironics is recalling Trilogy Evo ventilators (software v1.05.15.00) due to potential tidal volume delivery discrepancies.
4 products
FDA•CRITICALPhilips Respironics Trilogy Evo O2 VentilatorPhilips Respironics is recalling Trilogy Evo O2 ventilators (software v1.05.15.00) because the obstruction alarm may fail to trigger.
4 products
FSIS•MODERATEPunahele Jerky Company Beef CrispsPunahele Jerky Company beef crisps (6-oz and 4-oz packages) contain undeclared soy lecithin allergen; best-by date Feb 17, 2027 or prior.
FDA•Primal Herbs Dietary SupplementPrimal Herbs is recalling its dietary supplement due to the presence of undeclared sildenafil.
FDA•Rhino Choco VIP 10X ChocolateUSA LESS Co. is recalling Rhino Choco VIP 10X Chocolate due to the presence of undeclared tadalafil, a prescription drug ingredient.
FDA•MODERATESavannah Bee Company Honey BBQ Sauce MustardSavannah Bee Company is recalling Honey BBQ Sauce Mustard due to undeclared wheat and soy allergens caused by a mislabeling error.
FDA•MODERATEDivided Sunset Multi Collagen PeptidesDivided Sunset Multi Collagen Peptides are recalled for undeclared egg and fish allergens.
FDA•MODERATESIGNA Premier MR Scanner Magnet FittingsGE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.
FDA•CRITICALMedline NAMIC Angiographic Syringe KitsMedline is recalling NAMIC angiographic syringe kits due to a risk of the rotating adaptor disconnecting during use.
24 products
FDA•MODERATEOlympus SOLTIVE Premium Laser SystemOlympus is recalling the SOLTIVE Premium Laser System due to a power supply defect that may cause inoperability, smoke, or a burning smell.
2 products
FDA•MODERATECardinal Health Monoject Tuberculin Syringe 1 mLCardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.
FDA•MODERATESpacelabs Multi-parameter Command Module Model 91496Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.
FDA•MODERATEMedline Convenience Kits with 10mL SyringesMedline is recalling 10+ convenience kits containing 10mL syringes due to unapproved design changes.
21 products
FDA•Quest Cat Food Chicken RecipeGo Raw is recalling Quest frozen cat food due to potentially low levels of thiamine (Vitamin B1).
FDA•CRITICALHouse of Flavors Chicago Vanilla Ice CreamHouse of Flavors is recalling 3-gallon tubs of Chicago Vanilla Ice Cream due to an undeclared egg allergen.
FDA•MODERATEPepsin 1:3000 PowderAmerican Laboratories is recalling 50 kg drums of Pepsin 1:3000 Powder due to potential Salmonella contamination.
3 products
FDA•CRITICALButter-Rich PowderBluegrass Ingredients is recalling 50 lb. bags of Butter-Rich Powder due to potential Salmonella contamination.
2 products
FDA•MODERATELevothyroxine Sodium Tablets USP 150 mcgMacleods Pharma recalls Levothyroxine Sodium 150 mcg tablets (NDC 33342-401-44) nationwide due to subpotency.
FDA•MODERATENomida Semaglutide InjectionNew Life Pharma is recalling Nomida Semaglutide Injection due to a lack of assurance of sterility.
4 products
NHTSA•MODERATEAcura ZDX and Prologue Instrument Panel and Rearview Camera DisplayHonda is recalling 2024 Acura ZDX and Prologue vehicles for instrument panel display failure and rearview camera blank-screen defects that increase crash risk.
NHTSA•MODERATEBMW S 1000 RR Turn SignalBMW is recalling the 2026 S 1000 RR motorcycle due to turn signal malfunction that increases crash risk.
NHTSA•MODERATEBuick Regal Rear Toe LinkGM is recalling 2012–2013 Buick Regal Turbo and GS models over rear toe link fracture risk that may cause loss of vehicle control.
NHTSA•MODERATEGeneral Motors Multiple Models Electronic Owner's ManualGM recalling 2025–2027 Chevrolet, Cadillac, GMC, and Buick models over missing electronic owner's manual.
NHTSA•MODERATEIC Bus CESB School Bus Brake LinesInternational is recalling 2023–2027 IC Bus CESB school buses; brake lines may leak due to incorrect hardware installation.
FDA•Boner Bears Chocolate SyrupLockout Supplements is recalling Boner Bears Chocolate syrup due to the presence of undeclared sildenafil.
FDA•MODERATELowes Foods Sour Cream and Onion Potato ChipsLowes Foods sour cream and onion potato chips recalled for inaccurate nutrition labels and undeclared MSG.
FDA•CRITICALDreamland Zaatar Chickpea SaladDreamland is recalling Zaatar Chickpea Salad due to undeclared sesame, soy, and wheat allergens.
2 products
FDA•LOWC2O Coconut Water with PulpC2O Coconut Water with Pulp (17.5 oz) is recalled due to an incorrect ingredient label on the outer box that omits added sugar.
FDA•MODERATESynthes 2.4 Volt Locking Screw TapSynthes is recalling the 2.4 Volt Locking Screw Tap due to a labeling error that resulted in the inclusion of incorrect thread components.
2 products
FDA•MODERATEOlympus PKS Cutting ForcepsOlympus is recalling PKS Cutting Forceps (model 3005PK) because defective welds may cause the device's jaw to break during use.
7 products
NHTSA•MODERATEEvenflo LiteMax Factory Select Child SeatEvenflo LiteMax Factory Select (model CS100111198) recalled for incorrect weight/height limits in Spanish manual.
NHTSA•MODERATEToyota Corolla Headlight AssemblyToyota is recalling 2026 Corolla vehicles with missing headlight aim markings that may reduce visibility or create glare.
FDA•MODERATEMedline Namic GuidewiresMedline is recalling 50+ variants of Namic Guidewires due to the rescission of their 510(k) regulatory clearances.
28 products- Food RecallFDA•MODERATEGreenway Farms Jalapeno Dill Pickle Chips
Greenway Farms is recalling 16 fl oz Jalapeno Dill Pickle Chips due to the lack of a required process authority.
2 products 
FDA•MODERATEKing Harvest HummusKing Harvest is recalling Jalapeno and Roasted Red Pepper Hummus in 10 oz and 17 oz tubs due to potential aluminum piece contamination.
6 products
FDA•MODERATEImu-Tek Colostrum-5 CapsulesImu-Tek is recalling Colostrum-5 dietary supplement capsules due to the product being potentially under-processed.
2 products
FDA•MODERATEAmnesteem Isotretinoin Capsules 40 mgMylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.
NHTSA•MODERATENewmar Bay Star Hood StopNewmar is recalling 2018–2026 Bay Star motorhomes; hood stop adhesive may fail and detach during transit.
NHTSA•MODERATENewmar Freedom Aire Hydronic Heating SystemNewmar is recalling 2026 Freedom Aire motorhomes; hydronic heating system may unintentionally activate and produce harmful gas.
NHTSA•MODERATEThomas Built Buses Saf-T-Liner C2 Heater HoseDTNA is recalling 2027 Thomas Built Buses Saf-T-Liner C2 school buses over heater hose rupture risk and hot coolant leaks.
FDA•MODERATEStryker CHROMOPHARE Softlit Ring Surgical LightStryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System due to a potential failure of the ceiling cover support assembly.
NHTSA•CRITICALSubaru Crosstrek Hybrid and Forester Hybrid Fuel CapSubaru is recalling 2026 Crosstrek hybrid and 2025 Forester hybrid vehicles over fuel cap seal defect that may cause fuel leakage and fire risk.
NHTSA•MODERATEKia Telluride Front Seat Back FrameKia is recalling 2025 Telluride vehicles with power front seats due to seat back frame failure risk in crashes.
FDA•MODERATEAtellica CH Enzymatic Hemoglobin A1c (A1c_E)Siemens is recalling Atellica CH A1c_E assays due to a risk of depressed results when processed alongside RCRP on the same analyzer.
FSIS•CRITICALBremer Family Size Italian Style MeatballsRosina is recalling Bremer Family Size Italian Style Meatballs (32 oz, ~64 per package, BEST BY 10/30/26) over possible metal contamination.