NHTSA•MODERATE
Jaguar I-PACE High Voltage Battery
Jaguar is recalling 2020–2021 I-PACE vehicles; high voltage battery may overheat and catch fire.
Filters
Category
Agency
Severity
All Recalls
Back to home ←
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•LOWPitavastatin Tablets, 2 mgNorthstar Rx LLC is recalling Pitavastatin Tablets, 2 mg (NDC 72603-479-01) due to a foreign 1 mg tablet found in bottles.
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.
CPSC•Primark The Nightmare Before Christmas Glow-in-the-Dark Coloring SetPrimark is recalling The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets (code 0309401) due to high strontium and aluminum levels in crayons, posing a poisoning hazard to young children.
CPSC•Sunneday and Blue Bay Above-Ground PoolsStarmatrix Group recalls Sunneday and Blue Bay above-ground pools (models 70018, 70024, 358015W, 359015G, 360018W, 361018G, 380018T) over drowning hazard from compression strap footholds.
CPSC•NorthStar Hot Water Pressure WashersNorthStar is recalling three pressure washer models (items 157310, 157594, 157595) made Jan–Aug 2025 due to fan wheel failure risk causing flames and smoke.
CPSC•Urban Arrow FamilyNext Pro Cargo E-BikeGazelle USA recalls Urban Arrow FamilyNext Pro Cargo E-Bikes with defective Fidlock buckles that may fail to latch with children in cargo area.
CPSC•LuxJet Submersible LED LightsLuxJet Submersible LED Lights with accessible lithium coin batteries pose serious ingestion hazard to children; can cause internal burns and death.
CPSC•Bazic Silicone Glue Model 2030Bazic is recalling Silicone Glue Model 2030 (batch V01233-031725-70004523) over non-child-resistant packaging of methanol-containing product and incorrect labeling.
CPSC•Hobby Lobby Giraffe and Llama Plush Toys with ClipsHobby Lobby recalls Giraffe and Llama plush toys (models HL699436/HL731481) due to detachable legs releasing small beads—choking hazard.
CPSC•AiTuiTui Pull String Teething ToyAiTuiTui Pull String Teething Toy (Model 688-59) recalled for choking hazard; violates toy safety standards.
CPSC•Mindbodygreen Ultimate Multivitamin+ Dietary SupplementMindbodygreen recalls Ultimate Multivitamin+ bottles (UPC 850027975177, 850027975429) over non-child-resistant packaging containing iron.