CPSC•
Moodooy Adult Portable Bed Rails
Moodooy model F311 adult portable bed rails are recalled due to serious entrapment and asphyxiation hazards.
Filters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
CPSC•WonderStone Infant WalkersWonderStone infant walkers are recalled due to a fall hazard; they fail to meet mandatory safety standards for doorway and step-edge stopping.
FDA•MODERATEVersius Surgeon ConsoleCMR Surgical is recalling the Versius Surgeon Console due to a cybersecurity risk involving the Secure Boot feature.
- Device RecallFDA•MODERATETMINI Miniature Robotic System Tracking Arrays
Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays because a loose knob may cause surgical misalignment.
FDA•MODERATEVitek 2 AST-N447 Test KitBiomerieux is recalling Vitek 2 AST-N447 Test Kits due to potential for false resistant results caused by pouch foil fractures.
FDA•MODERATEOmniTract Surgical Retractor SystemIntegra LifeSciences is recalling the OmniTract Surgical Retractor System due to insufficient drying time instructions in the user manual.
FDA•MODERATEGSP Neonatal GALT KitThe GSP Neonatal GALT Kit is recalled due to reduced on-board stability, which may cause test failures and delays in patient results.
FDA•MODERATEFletcher CT/MR Shielded Applicator SetElekta recalls Fletcher CT/MR Shielded Applicator Set over risk of intrauterine tube tip detachment.
3 products
NHTSA•MODERATEVolvo VHD, VNL, VNR, VN, and VAH Steering KnucklesVolvo is recalling 2026 VHD, VNL, VNR, VN, and VAH trucks due to a risk of steering control loss from loose steering arm fasteners.
FDA•MODERATEPemetrexed for Injection 100mg/VialReliance Life Sciences recalls Pemetrexed for Injection 100mg/Vial over cGMP deviations.
4 products
FDA•MODERATEKlowen Custom Orthodontic SolutionKlowen is recalling the Custom Orthodontic Solution, model CIAS-800033, due to a defect that may cause incorrect bracket placement.
FDA•MODERATEAtellica CH Enzymatic Hemoglobin A1c AssaySiemens is recalling the Atellica CH Enzymatic Hemoglobin A1c assay (Material No. 11097536) due to potential for inaccurate patient results.
FDA•MODERATEMiniMed 780G Insulin PumpMedtronic is recalling MiniMed 780G Insulin Pumps due to a software error that can cause the device to unexpectedly stop delivering insulin.
FDA•MODERATEMedline Convenience KitsMedline recalls convenience kits with Covidien Mon-a-Therm probes due to distribution error.
3 products
FDA•MODERATEGasco Industrial: Multiple Isopropyl Alcohol ProductsGasco recalls Isopropyl Alcohol 70% in 16 oz, 32 oz, and 1 gal sizes due to subpotency.
6 products
FDA•MODERATEFresenius 5008X Blood Tubing SetsFresenius is recalling 5008X blood tubing sets due to potential connection errors between the tubing and the 5008X CAREsystem.
FDA•MODERATEIntracept Access InstrumentsBoston Scientific is recalling Intracept Access Instruments due to a potential sterile barrier breach that could lead to severe infection.
FDA•MODERATEEnovis EMPOWR 3D Knee InsertEncore Medical is recalling the EMPOWR 3D Knee Insert (11L 14MM) due to a packaging discrepancy involving incorrect product sizes.
2 products
FDA•MODERATEMasimo Radius VSM ECG Set and NIBP CuffMasimo recalls Radius VSM ECG Sets and NIBP Cuffs over false alarms and skin irritation risks.
2 products
NHTSA•CRITICALBMW Engine Starter RelayBMW is recalling certain 530e, 740Le, and 330e iPerformance vehicles due to an engine starter relay that may corrode and cause a fire.
FDA•LOWFexofenadine Hydrochloride Tablets 180 mgOhm Laboratories is recalling 180 mg Fexofenadine Hydrochloride tablets due to failed impurities and degradation specifications.
NHTSA•MODERATEHusqvarna and GasGas Motorcycle Rear Brake CaliperKTM is recalling certain Husqvarna and GasGas motorcycles because the rear brake caliper may crack and break, reducing braking ability.
NHTSA•MODERATEPeterbilt 579 and Kenworth T680 Air Brake ValvePACCAR is recalling certain 2026-2027 Peterbilt 579 and 2027 Kenworth T680 tractors due to an incorrectly installed air brake valve.
NHTSA•MODERATEForest River Wildwood and Salem Travel TrailersForest River is recalling 2026-2027 Wildwood and Salem travel trailers due to an incorrect GVWR on the Federal Placard.
NHTSA•MODERATEToyota and Lexus Rear Axle CarrierToyota is recalling 2026 Lexus TX and Toyota Grand Highlander vehicles due to a risk of rear axle carrier breakage and loss of vehicle control.
- Vehicle RecallNHTSA•MODERATEUtilimaster Velocity Strobe Light
Shyft is recalling 2016, 2019, and 2021 Utilimaster Velocity vehicles due to a strobe light short circuit that poses a fire risk.
NHTSA•MODERATEBMW Starter MotorBMW recalls certain 2023-2026 models over starter motor fire risk.
FDA•MODERATEApheresis Platelets, Leukocytes Reduced, IrradiatedVitalant is recalling Apheresis Platelets, Leukocytes Reduced, Irradiated due to missing white blood cell count verification testing.
FDA•CRITICALFresh & Ready Foods: 2 productsFresh & Ready Foods recalls Fresh to You chicken sandwiches due to possible Salmonella from raw patties.
2 products
FDA•CRITICALOrganic Moringa Leaf PowderTrafa Pharmaceuticals is recalling 15 kg bags of Organic Moringa Leaf Powder due to potential Salmonella contamination.
FDA•MODERATEMethohexital Sodium 100 mg/10 mLQuVa Pharma is recalling Methohexital Sodium 100 mg/10 mL vials due to failed impurities and degradation specifications.
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.