NHTSA•MODERATE
Ford Bronco Engine Compartment Wiring Harness
Ford recalls 2021-2026 Bronco and Bronco Raptor over wiring harness short circuit fire risk.
Filters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
NHTSA•MODERATEBlue Bird Vision Brake LineBlue Bird recalls 2022-2027 Vision buses over brake line damage that may cause fluid leak, fire, or crash risk.
- NHTSA•MODERATEBlue Bird Vision Brake Line
Blue Bird recalls 2022-2027 Vision school buses over brake line damage risk from cotter pin contact.
FDA•CRITICALZen Principle Moringa Leaf PowderZen Principle Moringa Leaf Powder recalled over possible Salmonella.
FDA•CRITICALCetirizine Hydrochloride Tablets 5 mgRising Pharma recalls Cetirizine HCl 5 mg tablets due to ranitidine cross-contamination.
FDA•CRITICALOLA-OLA Pounded Yam (Iyan)Fayus recalls OLA-OLA Pounded Yam for undeclared milk allergen.
FDA•CRITICALTaylor Farms de Mexico S. de: 21 productsTaylor Farms recalls 21 lettuce products over Cyclospora risk.
21 products
FDA•MODERATECyproheptadine Hydrochloride SyrupRising Pharma recalls Cyproheptadine HCl Syrup 2mg/5 mL due to crystallization and floating particles.
FDA•MODERATELevothyroxine Sodium Tablets 25 mcgMajor Pharmaceuticals recalls Levothyroxine 25 mcg tablets due to subpotency.
12 products
FDA•MODERATEAmlodipine and Olmesartan Medoxomil TabletsAscend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets (10 mg/20 mg) due to failed dissolution specifications.
FDA•LOWTrokendi XR Topiramate ER Capsules 25mgSupernus recalls Trokendi XR 25mg capsules over failed dissolution specs.
3 products
FDA•MODERATEVintage Roots Root Beer SyrupVintage Roots Root Beer Syrup recalled over unapproved sassafras bark additive.
FDA•LOWAscend Laboratories: Multiple Dabigatran Etexilate CapsulesAscend recalls Dabigatran etexilate capsules (110 mg, 150 mg) over impurity test failures.
2 products
FDA•MODERATEDivalproex Sodium Delayed-Release Tablets 500 mgBionpharma recalls Divalproex Sodium 500 mg tablets due to foreign tablets/capsules.
FDA•MODERATEFerno Power F2 Powered Fastening SystemFerno is recalling the Power F2 Powered Fastening System due to a risk of the rail mechanism lodging and preventing stretcher movement.
FDA•MODERATEHotline Fluid Warming SetICU Medical is recalling Hotline Fluid Warming Sets due to a risk of leakage at the tubing-to-connector bond.
FDA•MODERATEParagon 28 Phantom Intramedullary Nail System Guide RodParagon 28 is recalling the Phantom Hindfoot TTC/TC Ball Tipped Guide Rod (item P31-955-1800-S) due to sterile packaging breaches.
FDA•MODERATEBoston Scientific FARASTAR PFA GeneratorBoston Scientific is recalling FARASTAR PFA generators (Product ID 61M401) due to incompatibility with the FARAPOINT PFA catheter.
FDA•MODERATEFARASTAR Ablation Generator and FARAPOINT CatheterBoston Scientific recalls FARASTAR generator and ablation catheter due to missing IFU info for FARAPOINT catheter.
3 products
FDA•MODERATEApheresis Platelets, Leukocytes Reduced, IrradiatedLifeSouth is recalling Apheresis Platelets, Leukocytes Reduced, Irradiated, due to failure to meet platelet yield specifications.
NHTSA•MODERATEAltec AT Series Turntable FastenersAltec is recalling 2024-2026 AT Series vehicles due to improperly heat-treated turntable fasteners that may fail and cause separation.
FDA•MODERATEFARADRIVE Steerable Sheath Clear IDEBoston Scientific recalls FARADRIVE Steerable Sheath Clear IDE over valve damage risk that may cause air embolism.
4 products
NHTSA•MODERATEForetravel Realm Presidential Motorcoach MaxxAir Fan PCBForetravel recalls 2027 Realm Presidential Motorcoaches over MaxxAir fan PCB overheating fire risk.
2 products
NHTSA•MODERATEEvenflo Reo by Revolve360 Child Seat HeadrestEvenflo recalls Reo by Revolve360 child seats over headrest shift risk in a crash.
NHTSA•MODERATEGreat Dane Champion Dry Van Trailer Rear Impact GuardGreat Dane recalls 2027 Champion dry van trailers missing rear impact guard extension channels, increasing crash injury risk.
NHTSA•MODERATETurtle Top Terra Ford Transit Wheelchair LiftTurtle Top recalls 2026 Terra Ford Transit buses: wheelchair lift contactor may fail, causing unintended movement and injury risk.
FDA•MODERATETosoh ST AIA-Pack TestosteroneTosoh is recalling ST AIA-Pack Testosterone test kits due to potential for inaccurate results that may impact clinical treatment decisions.
NHTSA•CRITICALInternational MV and HV Battery Interconnect CableInternational is recalling certain MV and HV vehicles because the battery cable may short circuit, posing a fire risk.
NHTSA•MODERATEAltec AP45A Truck Boom Stow Switch WireAltec is recalling 2013-2025 AP45A trucks due to a damaged boom stow switch wire that may overheat and cause a fire.
NHTSA•MODERATEIC Bus EVSB and CESB School Bus Body PanelsInternational is recalling 2025-2027 IC Bus EVSB and CESB school buses due to body panel joints that may separate during a crash.
NHTSA•MODERATELand Rover Discovery Sport Rearview CameraLand Rover is recalling 2021-2025 Discovery Sport vehicles due to a rearview camera defect that may reduce driver visibility.
NHTSA•MODERATEJeep Gladiator and Wrangler Steel WheelsChrysler is recalling 2026 Jeep Gladiator and Wrangler vehicles due to steel wheels that may crack or detach, increasing crash risk.
2 products- NHTSA•MODERATEIC Bus CECB Body Panel Joints
IC Bus CECB buses recalled: body panel joints may lack epoxy, risking separation in crashes.
FDA•MODERATEBD ChloraPrep Clear ApplicatorsCareFusion is recalling BD ChloraPrep Clear sterile solution applicators due to a potential lack of sterility from incomplete packaging seals.
FDA•MODERATEPhotera 400 Phototherapy DeviceDaavlin recalls Photera 400 phototherapy device due to incorrect UV sensor gain causing inaccurate output.
3 products
FDA•MODERATEMedline Total Knee Pack Mixing Bowls and SpatulasMedline recalls Total Knee Pack kits with Zimmer Biomet mixing bowls and spatulas over sterility risk.
2 products
FDA•MODERATEVasoview Hemopro 2 Endoscopic Vessel Harvesting SystemVasoview Hemopro 2 Endoscopic Vessel Harvesting System is recalled due to an out-of-specification sterilization dose.
FDA•MODERATEMedtronic DLP Pediatric Arterial CannulaMedtronic recalls DLP Pediatric Arterial Cannula (CFN 77010) over loose foreign material with trace blood.
2 products
FDA•MODERATEPapablic Replacement Brush HeadsPapablic is recalling replacement brush heads over a choking hazard from breakage.
2 products
NHTSA•MODERATEOrange EV Terminal Truck Frame RailsOrange EV is recalling certain e-TRIEVER, T-Series, and HUSK-e terminal trucks due to frame rails that may crack and separate.
- Vehicle RecallNHTSA•MODERATEE-One Emergency Vehicles
E-One is recalling 2025-2026 Commercial, Typhoon N, and Cyclone N emergency vehicles due to a risk of sudden loss of drive power.
NHTSA•MODERATENissan Armada, Infiniti QX56, and QX80 Certification LabelsNissan is recalling certain Armada, QX56, and QX80 vehicles with 22-inch wheels due to incorrect GAWR labels that may lead to overloading.
FDA•MODERATECleviprex Injectable EmulsionChiesi USA is recalling Cleviprex (clevidipine injectable emulsion) 50 mg/100 mL vials due to a lack of assurance of sterility.
FDA•MODERATEAmy's Organic Lentil Soup Light in SodiumAmy's is recalling 14.5 oz cans of Organic Lentil Soup Light in Sodium due to potential spoilage.
FDA•MODERATEOla-Ola Pounded GroundnutsOla-Ola Pounded Groundnuts are recalled due to undeclared peanuts, posing a risk to consumers with peanut allergies.
FDA•MODERATEBell Pharmaceuticals: Multiple Carbamide Peroxide ProductsBell Pharmaceuticals recalls carbamide peroxide 6.5% earwax removers (CVS Health, Clinere, TopCare, etc.) for subpotency.
11 products
FDA•MODERATEWY Duck Sauce PacketsW.Y. Industries is recalling 0.35 oz. packets of WY Duck Sauce due to potential metal fragment contamination.
FDA•MODERATEOrthofix MINIRAIL Standard LengthenerOrthofix recalls MINIRAIL Standard Lengthener (M101) over incorrect labeling.
8 products
FDA•MODERATERuby Quartered Artichoke HeartsRuby Quartered Artichoke Hearts are being recalled due to potential glass contamination.
NHTSA•MODERATEWinnebago Navion and View Rooftop Ventilation FanWinnebago is recalling 2027 Navion and View RVs with MaxxAir N-Series rooftop fans due to an overheating circuit board fire risk.
2 products