NHTSA•MODERATE
Ford E-Transit High-Voltage Battery Pack
Ford is recalling 2026 E-Transit vehicles over missing washers in the high-voltage battery pack that may cause electrical arcing and fire.
Filters
Category
Agency
Severity
All Recalls
Back to home ←
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.
FDA•MODERATEPreema Bright Red and Orange Food Colour PowderPreema Bright Red and Orange Food Colour Powder recalled for banned carmoisine and undeclared FD&C Yellow 5 and Red 40.
2 products
FDA•MODERATEMetoprolol Succinate Extended-Release TabletsTeva is recalling Metoprolol Succinate Extended-Release Tablets due to failed dissolution specifications.
4 products
FDA•MODERATEOlympus Single Use Biopsy ValveOlympus is recalling the MAJ-210 single use biopsy valve due to the risk of rubber fragments detaching during use.
2 products
FDA•MODERATEParadise Ultrasound Renal Denervation CatheterReCor Medical is recalling the Paradise Ultrasound Renal Denervation Catheter (Model PRDS-068-02) as these units were not for human use.
3 products
NHTSA•MODERATEHonda and Acura Driver's Seat FrameHonda is recalling 2023 Accord, Accord Hybrid, and 2024 HR-V, Pilot, and Acura Integra vehicles due to improperly tightened driver's seat frames.
NHTSA•MODERATEJeep Grand Cherokee Rear Coil SpringsChrysler recalls 2021–2023 Jeep Grand Cherokee L and 2022–2023 Grand Cherokee over detachable rear coil springs.
NHTSA•MODERATEWinnebago Access Travel TrailerWinnebago is recalling 2026 Access travel trailers with missing Gross Axle Weight Rating labels.
NHTSA•MODERATEAutocar ACX Xpeditor Electronic Stability Control UnitAutocar is recalling 2023–2026 ACX Xpeditor vehicles; drive line yoke contact may damage the ESC unit and increase crash risk.
NHTSA•MODERATELamborghini Revuelto Rearview CameraLamborghini is recalling 2024–2025 Revuelto vehicles; rearview camera may not display due to software error.
- Device RecallFDA•MODERATEB. Braun Cesk Northside Anesthesia Tray
B. Braun is recalling the Cesk Northside Anesthesia Tray (Model 555076) due to potential cracking of the included adhesive tubing.
8 products 
FDA•Ashfiat Alharamain Honey Product for Energy SupportAkkarco is recalling Ashfiat Alharamain Honey Product for Energy Support due to the presence of the undeclared drug ingredient tadalafil.
FDA•CRITICALFrozen Fish BallsFrozen Fish Balls are being recalled due to undeclared wheat and sesame allergens.
3 products
FDA•CRITICALWhy Not Natural Moringa CapsulesWhy Not Natural is recalling Moringa Capsules due to potential Salmonella contamination.
FDA•MODERATEJiffy Original Composite Polisher Cups (Coarse)Ultradent is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011, due to crumbling and breakage risk.
FDA•MODERATEMedline Medcrest Surgical GownsMedline is recalling Medcrest surgical gowns due to a risk of fabric delamination during laundering, which may lead to infection.
3 products
NHTSA•MODERATEZero Motorcycles Front Brake HoseZero Motorcycles is recalling 2024–2025 DSR/X, DS, DSR, and DSRP motorcycles; front brake hose may leak, reducing braking ability.
NHTSA•MODERATEDucati Streetfighter V4 and Panigale V4 Rear Brake HoseDucati is recalling 2025–2026 Streetfighter V4 and Panigale V4 motorcycles due to rear brake hose damage from excessive heat.
NHTSA•MODERATEToyota Prius Rear Door LatchToyota is recalling 2023–2026 Prius models over rear door latch defect that may allow doors to open unexpectedly.
FDA•CRITICALHycoat Hyaluronate Sodium Sterile SolutionNeogen is recalling Hycoat Hyaluronate Sodium Sterile Solution for veterinary use due to potential microbial contamination.
2 products
FDA•Fu Zhou Fish BallsFu Zhou Fish Balls are recalled for undeclared sesame and wheat allergens.
FDA•MODERATEFrozen Half Shell OystersKhee Trading is recalling frozen half shell oysters due to potential Norovirus contamination.
FDA•MODERATEDiclofenac Sodium Topical Gel 3%Taro Pharmaceuticals is recalling Diclofenac Sodium Topical Gel 3% (100 g) due to viscosity specification failure.
FDA•CRITICALImpella RP Flex with SmartAssistAbiomed is recalling Impella RP Flex with SmartAssist devices due to a potential malfunction of the differential pressure sensor.
3 products
FDA•MODERATEBD 10mL Non-Sterile Luer-Lok SyringeBD is recalling 10mL non-sterile Luer-Lok syringes (catalog 301029) due to incorrect Luer Slip syringes mixed into batches.
FDA•MODERATELutronic CLARITY II Laser SystemLutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.
NHTSA•MODERATEHyundai Instrument Panel DisplayHyundai is recalling 2025–2026 Tucson, IONIQ 5, Santa Cruz, Kona, Palisade, Santa Fe, and Sonata vehicles over instrument panel display failure.
NHTSA•MODERATEKia Instrument Panel DisplayKia is recalling 2025–2026 K4, Sorento, Sportage, K5, EV9, and Carnival vehicles due to instrument panel display failure that may hide speedometer and warning lights.
FDA•MODERATEKeto-C Antiseptic WipesStratford Care USA is recalling Keto-C Antiseptic Wipes (50ct) due to misbranding; product contains non-medicated otic flush instead of labeled antiseptic.
36 products