FDA•MODERATE
Lidocaine HCl Injection USP
Spectra Medical Devices is recalling Lidocaine HCl Injection USP single-dose ampules due to a lack of assurance of sterility.
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All Recalls
Back to home ←- Food RecallFDA•MODERATEAlbertsons: multiple undeclared allergens
121 Albertsons products recalled for undeclared tree nuts, fish, or shellfish.
121 products 
FDA•LOWYunker Energy & Health Herbal SupplementSato Pharmaceutical is recalling Yunker Energy & Health Herbal Supplement due to a failure to meet label claims for Vitamin E content.
FDA•MODERATEAmlodipine and Olmesartan Medoxomil TabletsAscend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, due to failed dissolution specifications.
FDA•MODERATEArvis Hip & Knee 3.0 Instrument SetKico recalls Arvis Hip & Knee 3.0 Instrument Set over magnet face wear/corrosion.
2 products
FDA•MODERATEShimadzu X-Ray Systems High Voltage GeneratorShimadzu recalls X-ray systems over generator contactor weld risk; full model list on FDA page.
2 products
FDA•MODERATEDuloxetine DR Capsules 30 mgAsclemed USA is recalling Duloxetine DR Capsules 30 mg due to the presence of a nitrosamine impurity above acceptable intake limits.
NHTSA•MODERATEBraun Ram ProMaster Wheelchair Seat BeltBraun is recalling 2026 Ram ProMaster vehicles with Q'Straint wheelchair seat belts due to a risk of improper occupant restraint.
NHTSA•MODERATEKia Telluride Driver Seat Belt RetractorKia is recalling 2027 Telluride and Telluride Hybrid vehicles because the driver seat belt may fail to extend, increasing injury risk.
NHTSA•MODERATEChrysler Pacifica and Voyager Front Seat Harness ConnectorBraun is recalling 2023-2026 Chrysler Pacifica and Voyager vehicles due to a harness connector defect that may prevent air bag deployment.
NHTSA•MODERATENova Bus LFS and LFS Artic Transit BusesNova Bus is recalling LFS and LFS Artic transit buses (1997-2024) because the low brake air pressure warning light may fail to illuminate.
FDA•MODERATEPhaseOne Antimicrobial Solution SprayerOculus Technologies is recalling PhaseOne Antimicrobial Solution due to sprayer spring corrosion that may contaminate the product.
FDA•MODERATECASE v7.0 Cardiac Testing SystemGE Medical is recalling the CASE v7.0 Cardiac Testing System due to a risk of electrical sparking at the printer head.
FDA•MODERATEHiRes Ultra 3D CI HiFocus Mid Scala Cochlear ImplantAdvanced Bionics is recalling the HiRes Ultra 3D CI HiFocus Mid Scala cochlear implant due to an incorrect shelf-life expiration date.
2 products
FDA•MODERATENeptune Smart Docking StationStryker is recalling the Neptune Smart Docking Station (120V) due to missing safety testing and a potential electrical shock risk.
FDA•MODERATECovidien EndoStitch Polysorb Single Use Loading UnitCovidien is recalling EndoStitch Polysorb loading units (170053, 170071) due to packaging holes that may compromise sterility.
NHTSA•MODERATEGrand Design Reflection Fifth Wheel Shock BoltsGrand Design is recalling 2025-2026 Reflection fifth wheel trailers over incorrectly tightened shock bolts that may detach while driving.
FDA•MODERATEMotor City Pizza Co. 5 Cheese BreadMotor City Pizza Co. 5 Cheese Bread recalled over potential Salmonella contamination.
FDA•LOWLidocaine HCl Injection 2%Eugia US LLC is recalling Lidocaine HCl Injection 2% because the label wrap covers the barcode, making it difficult to scan.
- Device RecallFDA•MODERATEB. Braun CESK Northside Anesthesia Tray
B. Braun recalls CESK Northside Anesthesia Tray due to cracked adhesive tubing.
8 products 
FDA•MODERATECovidien Mon-a-Therm Esophageal StethoscopeCovidien recalls Mon-a-Therm Esophageal Stethoscope 400TM (REF 90042) due to lack of FDA clearance.
3 products
FDA•MODERATEExacta Mix Vented Micro-Volume InletBaxter is recalling Exacta Mix Vented Micro-Volume Inlet (Model H938175) due to incorrect filters that may cause flow and clinical issues.
FDA•MODERATECovidien Shiley Tracheostomy TubeCovidien is recalling Shiley Tracheostomy Tubes due to incorrect display box labeling.
FDA•MODERATEIvenix Infusion System Large Volume PumpFresenius Kabi is recalling the Ivenix Infusion System LVP due to a risk of the cassette loading lever breaking during use.
NHTSA•MODERATEForest River Wildwood and Salem Travel TrailersForest River is recalling 2024-2025 Wildwood and Salem travel trailers due to a fire hazard from incorrectly wired fireplace outlets.
NHTSA•MODERATEMercedes-Benz GLE and GLS Rear Seat Belt BoltsMercedes-Benz is recalling various 2026 GLE and GLS models because rear seat belt bolts may be loose, increasing the risk of injury in a crash.
CPSC•MiniWarGaming and Primal Horizon Disc MagnetsThese magnets pose a serious ingestion hazard to children, as they can attract each other or other metal objects if swallowed, potentially causing intestinal perforation, blockage, or death.
CPSC•Panasonic Lithium Coin BatteriesPanasonic VL2020 lithium coin batteries are recalled for lacking child-resistant packaging, posing a severe ingestion and chemical burn risk.
CPSC•Anzmtosn Luminous Fidget Spinner BallsAnzmtosn is recalling Luminous Fidget Spinner Balls (Model FS0862) because the included flashlight batteries pose a serious ingestion hazard.
CPSC•Misco Sports Light-Up Racket SetsMisco Sports Light-Up Racket Sets (model MT2287) are recalled due to a battery ingestion hazard that can cause serious injury or death.
CPSC•Mainstays 9-Drawer Fabric DressersMainstays 9-Drawer Fabric Dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.
FDA•MODERATEMedtronic 1x4 Pocket Adaptor KitMedtronic recalls 1x4 Pocket Adaptor Kit (Model 64001) due to incorrect Use-By-Dates.
2 products
FDA•MODERATEMedline Eye Tray-LF Convenience KitMedline is recalling Eye Tray-LF kits containing mislabeled Cardinal Health syringes that may lead to incorrect insulin dosing.
FDA•MODERATEPhilips Azurion System HDDPhilips recalls Azurion systems over aging HDDs that may cause loss of imaging or movement.
3 products
NHTSA•MODERATEARBOC Transit Bus Wheelchair Restraint RetractorARBOC is recalling certain 2025-2026 transit buses because the wheelchair restraint retractors may not lock, increasing the risk of injury.
NHTSA•MODERATEIC Bus EVSB Drive Motor Mounting BracketInternational is recalling 2026-2027 IC Bus EVSB school buses because the drive motor may detach due to improperly tightened mounting bolts.
NHTSA•MODERATEForest River Bus Wheelchair Restraint RetractorForest River Bus is recalling various 2025-2027 bus models due to QRT-3 wheelchair retractors that may fail to lock, increasing injury risk.
NHTSA•MODERATESubaru Forester Power MoonroofSubaru is recalling 2026 Forester and Forester Hybrid vehicles because the power moonroof glass may detach, creating a road hazard.
NHTSA•MODERATEChevrolet Express and GMC Savana Steering ColumnGM is recalling 2026 Chevrolet Express and GMC Savana vehicles due to a steering column defect that may cause inaccurate gear selection.
FDA•LOWPred Mild Ophthalmic SuspensionAbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.
FDA•MODERATEHydroMARK Breast Biopsy Site MarkerDevicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.
NHTSA•MODERATETiffin Open Trail, Wayfarer, and Midas Recreational VehiclesTiffin is recalling 2026-2027 Open Trail, Wayfarer, and 2026 Midas RVs due to non-compliant cargo capacity labels that may increase crash risk.
NHTSA•MODERATEEmber Touring Edition Recreational Trailer Shock BoltsEmber is recalling 2026-2027 Touring Edition trailers due to improperly tightened shock bolts that may detach and create a road hazard.
NHTSA•MODERATELexus and Toyota Instrument Panel ClusterToyota is recalling various Lexus and Toyota models because the instrument panel may fail to display critical safety warnings.
NHTSA•MODERATEFord Expedition and Lincoln Navigator Seat Belt PretensionerFord is recalling 2018-2022 Expedition and Lincoln Navigator vehicles due to a seat belt pretensioner defect that may prevent proper restraint.
NHTSA•MODERATEFord Explorer, Ranger, and Bronco EngineFord is recalling 2025-2026 Explorer, Ranger, and Bronco vehicles due to an engine failure risk that may cause a loss of drive power.
FDA•LOWNicotine Transdermal System Patch 14 mgAveva is recalling 14 mg Nicotine Transdermal System Patches due to elevated levels of oxidative-related impurities.
NHTSA•MODERATEAlliance Paradigm Curt Touring Coil Suspension Shock BoltsAlliance is recalling 2025-2027 Paradigm trailers with Curt Touring Coil Suspensions due to a risk of detached shock bolts causing road hazards.
NHTSA•MODERATEForest River Recreational Trailer Shock BoltsForest River is recalling certain 2026 Riverstone, 2026 Cedar Creek, and 2024 R-Pod trailers due to incorrectly tightened shock bolts.
NHTSA•MODERATEFord Ranger and Bronco Tire Placard LabelsFord is recalling 2026 Ranger and Bronco vehicles due to incorrect tire and weight capacity information on safety labels.