FDA•MODERATE
Methohexital Sodium 100 mg/10 mL
QuVa Pharma is recalling Methohexital Sodium 100 mg/10 mL vials due to failed impurities and degradation specifications.
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FDA•MODERATEVanilla Dessert ShellsSpecialty Bakers is recalling Vanilla Dessert Shells due to an undeclared soy allergen.
FDA•MODERATEAlabama Banana Pudding MarshmallowWondermade is recalling 4 oz packages of Alabama Banana Pudding Marshmallow due to potential metal contamination.
FDA•MODERATEMedline Remedy Specialized Silicone CreamMedline Remedy Specialized Silicone Cream is recalled due to an out-of-specification result for formaldehyde in the raw material.
FDA•MODERATEClomiphene Citrate USP Active Pharmaceutical IngredientShimoga Chemicals is recalling Clomiphene Citrate USP Active Pharmaceutical Ingredient due to cGMP deviations.
FDA•MODERATESuper Healthy Hair Blow Dry SprayBeauty Pie is recalling Super Healthy Hair Blow Dry Spray (150 ml) due to potential contamination with Pseudomonas aeruginosa.
FDA•MODERATEMethohexital Sodium for Injection 500 mgAvet Pharmaceuticals is recalling Methohexital Sodium for Injection 500 mg vials due to failed impurities and degradation specifications.
FDA•MODERATEAquacel Ag Surgical SP DressingConvaTec is recalling Aquacel Ag Surgical SP dressings because they were manufactured with a thickness exceeding specifications.
FDA•MODERATEWise Onion RingsWise Foods is recalling 3.75 oz bags of Onion Rings due to undeclared colors and the presence of an unapproved color additive.
FDA•MODERATEOlympus Single Use Distal CoverOlympus is replacing the previous design of the MAJ-2315 Single Use Distal Cover used with the EVIS EXERA III Duodenovideoscope.
NHTSA•MODERATEBraun Chevrolet Traverse Fuel Fill LineBraun is recalling 2026 Chevrolet Traverse vehicles due to a missing braze connection in the fuel fill line that poses a fire risk.
NHTSA•MODERATEKenway Towing Light Kits and Submersible LightsHarbor Freight is recalling Kenway towing and submersible lights that may fail to illuminate, increasing the risk of a crash.
NHTSA•MODERATESubaru Crosstrek, Forester, and Ascent Certification LabelsSubaru is recalling various Crosstrek, Forester, and Ascent models due to incorrect weight rating labels that may lead to vehicle overloading.
NHTSA•MODERATEWabash Econex Refrigerated Body Side Door StepWabash is recalling 2021-2026 Econex Refrigerated Body vehicles because the side door stirrup steps may detach, posing injury and crash risks.
FDA•Ola-Ola Pounded YamOla-Ola Pounded Yam is recalled due to undeclared milk, which poses a risk to consumers with milk allergies.
- FDA•Ola-Ola Pounded Yam
Ola-Ola Pounded Yam recalled for undeclared milk allergen.
FDA•CRITICALAdams Extract & Spice: 5 productsAdams Extract & Spice recalls 5 seasoning and mix products over undeclared sesame allergen.
5 products
NHTSA•MODERATEQ'Straint Max Wheelchair RetractorPrime-Time is recalling Q'Straint Max wheelchair retractors in 2025-2026 Ford Med Transit vans that may fail to lock and secure wheelchairs.
NHTSA•MODERATEToyota Tundra Load Carrying Capacity LabelSoutheast Toyota is recalling one 2026 Tundra truck due to an incorrect load carrying capacity label that violates federal safety standards.
FDA•CRITICALOrganic Whole BlueberriesFrutas y Hortalizas del Sur S.A. is recalling 10 oz bags of Organic Whole Blueberries due to potential E. coli O145:H28 contamination.
FDA•MODERATEPedigree High Protein Chopped Ground DinnerMars Petcare is recalling Pedigree High Protein Chopped Ground Dinner over potential contamination with plastic and metal foreign material.
FDA•CRITICALFusia Asian Inspirations Kimchi & Tofu KimbapFusia Kimchi & Tofu Kimbap recalled due to undeclared fish allergen.
FDA•MODERATECinacalcet Hydrochloride Tablets 30 mgCipla recalls Cinacalcet HCl 30 mg tablets over N-nitroso impurity above safe limit.
3 products
FDA•MODERATEDextroamphetamine/Amphetamine Extended-Release CapsulesLannett is recalling 5 mg Dextroamphetamine/Amphetamine ER capsules due to a labeling mix-up where capsules contain immediate-release pellets.
FDA•MODERATEAsclemed: Multiple Lidocaine Hcl Injection ProductsAsclemed recalls Accucaine kits and Lidocaine HCl injection ampules over sterility concerns.
2 products
FDA•MODERATEA.T.S. 4000 TS Tourniquet Dual HoseZimmer Surgical recalls A.T.S. 4000 TS Tourniquet Dual Hoses over sterility breach risk.
2 products
FDA•MODERATEGore TAG Thoracic Branch Endoprosthesis Side Branch ComponentGore is recalling 30+ models of the TAG Thoracic Branch Endoprosthesis Side Branch Component due to a risk of catheter separation.
2 products
FDA•CRITICALReprocessed Electrophysiology and Ultrasound CathetersMedline is recalling reprocessed catheters due to residual particulate matter that may cause infection or embolism.
FDA•MODERATEBard Acute Drainage TraysBard recalls Acute Drainage trays due to deficient lidocaine ampoules from supplier.
20 products
FDA•MODERATEMedline Gravity SetMedline is recalling gravity sets labeled "Not for Human Use" that were inadvertently shipped to the U.S. market.
FDA•CRITICALMedtronic Harmony Delivery Catheter SystemMedtronic is recalling the Harmony Delivery Catheter System due to a manufacturing defect that may cause the distal tip to detach during use.
FDA•MODERATESolar GI System Water PerfusionLaborie is recalling Solar GI System configurations due to moisture accumulation that may affect pressure measurement performance.
FDA•MODERATECovidien Shiley Disposable Decannulation PlugCovidien is recalling 12+ models of Shiley Disposable Decannulation Plugs due to incorrect labeling regarding DEHP content.
2 products
NHTSA•MODERATEJayco Heartland Cyclone Travel and Fifth Wheel TrailersJayco is recalling 2026 Heartland Cyclone trailers due to a missing inverter ground connection that poses fire and electrical shock risks.
NHTSA•MODERATEJayco Seismic Fifth Toy HaulersJayco is recalling 2026 Seismic fifth toy haulers due to a missing grounding connection that poses fire and electrical shock risks.
NHTSA•CRITICALKia Telluride Power Seat MotorKia is recalling 2020-2024 Telluride vehicles due to a risk of fire from overheating front power seat motors.
NHTSA•CRITICALHyundai Ioniq 5 High Voltage BatteryHyundai is recalling 2023-2024 Ioniq 5 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.
NHTSA•CRITICALKia EV6 and EV9 High Voltage BatteryKia is recalling 2022-2024 EV6 and 2024 EV9 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.
- Vehicle RecallNHTSA•MODERATEAltec Service Body Inverter AC Wiring
Altec is recalling 2022-2026 Service Body vehicles due to a wiring defect that may cause a short circuit and increase the risk of fire.
NHTSA•MODERATENissan Leaf Rear Seat Belt RetractorsNissan is recalling 2026 Leaf vehicles because rear seat belt retractors may fail to properly secure child restraint systems.
NHTSA•CRITICALCrestline Ford CCL166 Type III Emergency VehicleCrestline is recalling 2026 Ford CCL166 Type III emergency vehicles due to a fuel line puncture risk that may cause a fire.
NHTSA•MODERATEWarn Wireless Remote KitsWarn is recalling wireless remote kits (part numbers 90287 and 90289) that may cause unexpected winch movement, posing an injury risk.
FDA•Eunha Fisheries Sliced Korean Halibut and Flounder SashimiEunha Fisheries recalls frozen halibut and flounder sashimi due to undeclared wheat, soy, and sesame allergens.
FDA•MODERATEGlucagon Emergency KitLupin recalls Glucagon Emergency Kits due to a stability test failure that may impair emergency use.
3 products
FDA•MODERATEProvision Health: 2 productsPH Labs recalls Ocular Plus and Vista MAX supplements for undeclared Yellow #5 allergen.
2 products
FDA•MODERATEGemcitabine InjectionHikma is recalling Gemcitabine Injection due to improper temperature storage.
FDA•MODERATEZeiss Intrabeam Spherical ApplicatorZeiss is recalling the 1.5 cm Intrabeam Spherical Applicator (REF 304534-6000-557) due to failure to meet manufacturing specifications.
FDA•MODERATESiemens ARTIS icono Ceiling SuspensionSiemens is recalling the ARTIS icono ceiling suspension (Model 11328100) because monitor attachment screws may loosen over time.
FDA•CRITICALDSAEK Pack-RX Surgical Convenience KitWindstone Medical recalls DSAEK Pack-RX kits due to contaminated alcohol prep pads.
4 products- Device RecallFDA•MODERATERayCare 2024A SP1 Oncology Information Systems
RaySearch recalls RayCare 2024A SP1 over beam set delivery note data loss risk.
2 products