FDA•LOW
Lidolog Kit
Lidolog Kit is being recalled because the label wrap obscures the barcode, making it difficult to scan.
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FDA•MODERATEOlympus 4K UHD LCD MonitorOlympus is recalling the 4K UHD LCD Monitor (model OEV321UH) due to a potential connector fault that may cause image loss or abnormalities.
FDA•MODERATEFARADRIVE Steerable Sheath Clear IDEBoston Scientific is recalling the FARADRIVE Steerable Sheath Clear IDE due to potential valve damage that may cause air embolism.
4 products
FDA•MODERATEAVID Medical Eye Pack Convenience KitAVID Medical is recalling the Eye Pack convenience kit (Model LVEY27) due to an incorrect concentration of Betadine solution.
FDA•MODERATESeaSpine Polyaxial HeadSeaSpine is recalling the Polyaxial Head due to a manufacturing error that may cause the component to detach during surgery.
NHTSA•MODERATEFord Bronco Engine Compartment Wiring HarnessFord recalls 2021-2026 Bronco and Bronco Raptor over wiring harness short circuit fire risk.
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•Zen Principle Moringa Leaf Powder CapsulesZen Principle Moringa Leaf Powder Capsules recalled over possible Salmonella contamination.
FDA•Cetirizine Hydrochloride Tablets 5 mgCetirizine HCl 5 mg tablets recalled over possible Ranitidine cross contamination; lots GY825029–GY825032.
FDA•Ola-Ola Pounded YamFayus recalls Ola-Ola Pounded Yam (2lb–10lb) for undeclared milk allergen.
FDA•Taylor Fresh Foods Iceberg LettuceTaylor Fresh Foods recalls iceberg lettuce under CV, JB, Mark, MKTSD brands due to Cyclospora risk.
FDA•MODERATECyproheptadine Hydrochloride SyrupRising Pharma recalls Cyproheptadine HCl Syrup 2mg/5 mL due to crystallization and floating particles.
FDA•MODERATELevothyroxine Sodium 25 mcg TabletsMajor Pharmaceuticals is recalling Levothyroxine Sodium 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•Trokendi XR 25mg CapsulesSupernus Pharmaceuticals is recalling Trokendi XR 25mg capsules due to failed dissolution specifications.
FDA•MODERATEVintage Roots Root Beer SyrupVintage Roots is recalling 8 oz Root Beer Syrup due to the presence of an unapproved food additive, sassafras bark.
FDA•Ascend Laboratories: Multiple Dabigatran Etexilate CapsulesAscend Laboratories is recalling 110 mg and 150 mg Dabigatran etexilate capsules due to failed impurity and degradation specifications.
2 products
FDA•Divalproex Sodium Delayed-Release TabletsBionpharma is recalling 500 mg Divalproex Sodium Delayed-Release Tablets due to the presence of foreign tablets or capsules in the bottles.
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 Cardiac Ablation CatheterBoston Scientific is recalling FARASTAR Ablation Generators and Cardiac Ablation Catheters due to missing information in the device labeling.
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.
NHTSA•MODERATEForetravel Realm Presidential Motorcoach MaxxAir Fan PCBForetravel recalls 2027 Realm Presidential Motorcoaches over MaxxAir fan PCB overheating fire risk.
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.
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•MODERATEInternational MV and HV Battery CableInternational is recalling certain 2021, 2023-2027 MV, and 2026-2027 HV vehicles due to a short circuit risk in the battery interconnect cable.
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.
FDA•Khong Guan Glutinous Rice Balls with Black Sesame FillingKhong Guan expands recall of glutinous rice balls with black sesame filling due to undeclared peanuts.
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 wrong output.
3 products
FDA•MODERATEMedline Total Knee Pack DYNJT6267Medline recalls Total Knee Pack DYNJT6267 over sterility breach risk from Zimmer Biomet mixing bowls and spatulas.
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 One-Piece Pediatric Arterial CannulaMedtronic recalls DLP Pediatric Arterial Cannula (CFN 77010) over loose foreign material risk.
2 products
FDA•MODERATEPapablic Replacement Brush HeadsPapablic recalls Replacement Brush Heads model Papablic18B due to breakage risk.
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 store-brand carbamide peroxide ear drops for subpotency (low pH, ~0.6% assay).
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.