FDA•MODERATE
Ivenix Infusion System Large Volume Pump
Fresenius Kabi is recalling the Ivenix Infusion System LVP due to a risk of the cassette loading lever breaking during use.
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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•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•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•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•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•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•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
FDA•MODERATERepackaged M&Ms Peanut CandiesBeacon Promotions is recalling 1.3 oz repackaged M&Ms Peanut candies due to undeclared milk, soy, and peanut allergens.
3 products
FDA•MODERATEGerber Arrowroot BiscuitsGerber Arrowroot Biscuits (5.5 oz, UPC 015000005962) recalled for potential paper/plastic contamination in arrowroot flour.
FDA•MODERATEAsteria Health Testosterone Sterile PelletsAsteria Health is recalling 100 mg testosterone pellets due to potential metal particulate contamination.
25 products