CPSC•
YITA 16-Drawer Dressers (Multiple Brands)
YITA is recalling 16-drawer dressers (Dextrus, ModFusion, Uforic, Yintatech, Yitahome) due to tip-over and entrapment hazards; wall anchoring required.
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CPSC•Lotus Joy Sweet Birch Essential OilLotus Joy Sweet Birch Essential Oil recalled for lack of child-resistant packaging; methyl salicylate poisoning risk.
CPSC•Shintenchi 6-Drawer DresserShintenchi 6-drawer dresser (model SHX12077-WH) recalled for tip-over and entrapment hazards; requires wall anchoring.
CPSC•Semfri Children's HelmetsSemfri children's helmets (size M) sold at Walmart.com June–Nov 2025 fail safety standards and pose serious head injury risk.
CPSC•Lola + The Boys Youth Hooded Clothing with DrawstringsLola + The Boys is recalling five youth hooded clothing styles with drawstrings due to strangulation hazard in children.
CPSC•Kitosun Submersible LED LightsKitosun Submersible LED Lights recalled for easily accessible lithium coin batteries posing serious ingestion hazard to children.
CPSC•Organic Zing Birch Essential Oil BottlesOrganic Zing Birch Essential Oil bottles lack required child-resistant packaging, posing poisoning risk to children.
FDA•MODERATETippy Toes Apple Pear Banana Baby FoodTippy Toes Apple Pear Banana baby food is recalled due to potential patulin contamination.
FDA•MODERATEThiamine HCl InjectionFagron Sterile Services is recalling Thiamine HCl 500 mg injection due to a lack of assurance of sterility.
5 products
FDA•MODERATECampy CVA MediumRemel is recalling Campy CVA Medium (R01272) due to low recovery of Campylobacter Jejuni on identified lots.
NHTSA•MODERATEJaguar I-PACE High Voltage BatteryJaguar is recalling 2020–2021 I-PACE vehicles; high voltage battery may overheat and catch fire.
FDA•MODERATESTA Liatest D-Di KitDiagnostica Stago is recalling the STA Liatest D-Di kit due to a positive bias that may cause inaccurate D-Dimer test results.
2 products
CPSC•Scepter B62 Fuel ContainersScepter B62 fuel containers lack flame mitigation and child-resistant spouts, posing flash fire and burn risks.
FDA•MODERATEDexamethasone Sodium Phosphate Injection, USP 100 mg/10 mLSomerset Therapeutics is recalling Dexamethasone Sodium Phosphate Injection (NDC 70069-025-10/01) due to out-of-specification impurities at expiry.
FDA•MODERATESTA Liatest Free Protein SDiagnostica Stago is recalling STA Liatest Free Protein S kits due to the risk of inaccurate test results for normal patient plasma levels.
NHTSA•MODERATEFreightliner Business Class M2 Steering GearboxFontaine Modification is recalling 2024–2025 Freightliner Business Class M2 vehicles over insufficient steering gearbox oil that may cause steering difficulty.
NHTSA•MODERATEMercedes Benz Tourrider Transit Bus Door Control ValveDaimler Coaches is recalling 2026 Mercedes Benz Tourrider transit buses with defective door control valves that may prevent door opening.
NHTSA•MODERATEEmber 2026 E-Series and Overland Series Travel TrailersEmber is recalling 2026 E-Series and Overland Series travel trailers with incorrect cargo capacity labels that may cause overloading.
NHTSA•MODERATEBMW 228i and M235i Gran Coupe Rear LightsBMW is recalling 2026 228i and M235i Gran Coupe vehicles with rear lights that may not function properly, increasing crash risk.
FDA•MODERATEReact Health PHOENIX 5L Oxygen ConcentratorReact Health PHOENIX 5L Oxygen Concentrator recalled due to devices not meeting quality specifications.
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.
FSIS•CRITICALMays Chemical Company Frozen Pork Boneless LoinsMays Chemical recalls 46,315 lbs of frozen pork boneless loins imported without U.S. reinspection; discard or return.
FDA•MODERATEPure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep ResetPure Solutions recalling 1 fl oz sleep formula bottles due to undeclared milk allergen from bovine colostrum.
FDA•MODERATECoco's Italian Market Cannoli Making KitCoco's Italian Market is recalling Cannoli Making Kits due to undeclared wheat and milk allergens.
2 products
FDA•CRITICALPrime Food Processing Dried Croaker FishPrime Food Processing is recalling Dried Croaker Fish due to the risk of botulism from uneviscerated fish.
FDA•MODERATEEquinoxe Ergo Modular Impactor HandleExactech is recalling the Equinoxe Ergo Modular Impactor Handle due to a missing cross-pin that may cause device failure.
2 products
FDA•MODERATEImactis CT-Navigation SystemGE Medical Systems is recalling Imactis CT-Navigation System (Models E85101LA, E85101LP) due to potential needle trajectory/tip position discordance.
FDA•MODERATEIBA Proton Therapy System PROTEUS 235IBA PROTEUS 235 proton therapy systems may fail to stop beam delivery if external gating device signal is lost, risking patient mistreatment.
NHTSA•MODERATEFord E-Transit High-Voltage Battery PackFord is recalling 2026 E-Transit vehicles over missing washers in the high-voltage battery pack that may cause electrical arcing and fire.
NHTSA•MODERATEFord Transit Engine CrossmemberFord is recalling 2023–2024 Transit vehicles over improperly secured engine crossmember that may cause loss of drive power or brake failure.
FDA•MODERATEPro Numb Tattoo Numbing SprayPro Numb is recalling 5% Lidocaine Tattoo Numbing Spray due to cGMP manufacturing deviations.
2 products
FDA•MODERATEB. Braun Winged Infusion SetsB. Braun is recalling 21GA Winged Infusion Sets (Model 7M2802) due to potential needle tip dullness or breakage.
3 products
FDA•MODERATEMICS3 Angled Sagittal Saw AttachmentHowmedica Osteonics is recalling MICS3 Angled Sagittal Saw Attachments because external screws may loosen and detach during use.
NHTSA•MODERATEChrysler Trailer Tow ModuleChrysler is recalling 2024–2026 Jeep Wagoneer S and Ram pickup/cab chassis vehicles over trailer tow module defects causing brake light and brake failure.
- Equipment RecallNHTSA•MODERATEMopar Tow Trailer Module
Chrysler is recalling Mopar tow trailer modules that may cause trailer lights and brakes to fail, increasing crash risk.
NHTSA•MODERATEPierce 2025 Velocity/Saber/Impel/Enforcer/Arrow XT Steering Linkage ArmPierce is recalling 2025 Velocity, Saber, Impel, Enforcer, and Arrow XT vehicles due to steering linkage arm detachment risk.
FDA•MODERATEOn-X Mitral Heart Valve with Conform-X Sewing RingOn-X is recalling Model ONXMC-25/33 Mitral Heart Valve due to incomplete testing before distribution.
FDA•CRITICALKirkland Signature Mini BeignetsKirkland Signature Mini Beignets are recalled due to undeclared hazelnut, posing a risk to those with hazelnut allergies.
FDA•CRITICALMolly Kitchen's Tuna SaladReser's Fine Foods is recalling Molly Kitchen's Tuna Salad due to undeclared fish allergen from incorrect lid labeling.
2 products
FDA•CRITICALKarns Foods Mini Dark Chocolate Raspberry CupsKarns Foods is recalling 8 oz Mini Dark Chocolate Raspberry Cups due to undeclared peanuts.
FDA•MODERATETiki Bar Dark Chocolatey Peanut Butter & PretzelTiki Bar Dark Chocolatey Peanut Butter & Pretzel is recalled due to an undeclared peanut allergen.
FDA•MODERATEBeckman Coulter Chemistry AnalyzersBeckman Coulter is recalling chemistry analyzers due to a software error that may cause system delays and impact patient diagnosis.
2 products
FDA•MODERATEMedline Cardiac Procedure KitsMedline is recalling cardiac procedure kits to clarify that the included chest drainage units are intended for adult patients only.
FDA•MODERATEMiniMed 780G Insulin PumpMedtronic is recalling MiniMed 780G insulin pumps (models MMT-1884, MMT-1886) running software 6.60-6.62 due to insulin delivery inaccuracies.
- Device RecallFDA•MODERATECentricity Universal Viewer Software
GE is recalling Centricity Universal Viewer software versions 5.0 and 7.0 due to a cybersecurity vulnerability that may expose user credentials.
4 products - Device RecallFDA•MODERATEHealthCast Vital Sync Remote Patient Monitoring System
Covidien is recalling Vital Sync software because patient bedside monitor alarms may fail to transmit to the remote monitoring system.
2 products 
NHTSA•CRITICALGrand Design Solitude Water Tank Heating PadGrand Design is recalling 2026 Solitude RVs with ThermaHeat Tank Pad due to fire risk from heating pad failure.
NHTSA•MODERATEGrand Design Lineage Motorhome Driver and Passenger Seat BaseGrand Design is recalling 2025–2026 Lineage motorhomes with loose driver and passenger seat bases that increase crash injury risk.
NHTSA•MODERATEBMW Starter MotorBMW is recalling 2021–2024 3/4/5 Series, X3, X4, Z4, and Supra models due to starter motor fire risk.
FDA•MODERATETandem Insulin Infusion PumpTandem is recalling insulin infusion pumps in Czech Republic and Slovakia due to user guide translation errors that could cause unintended insulin delivery.