NHTSA•MODERATE
Jeep Wagoneer S Liftgate Hinge Cover
Chrysler is recalling 2024–2026 Jeep Wagoneer S vehicles; liftgate hinge cover may detach and create a road hazard.
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NHTSA•MODERATEGillig Low Floor Transit Bus High Voltage CableGillig is recalling 2023–2026 Low Floor transit buses over high voltage cable overheat and fire risk.
FDA•MODERATEB.R.A.H.M.S PlGF Plus KRYPTOR In Vitro Diagnostic TestB.R.A.H.M.S PlGF Plus KRYPTOR (Catalog 859075N) recalled for out-of-range quality control values that may cause falsely elevated preeclampsia risk results.
FDA•MODERATEStryker Sustainability Solution Tourniquet CuffsStryker is recalling tourniquet cuffs that may fail to maintain pressure due to a potential detachment at the welding connection.
FDA•MODERATEARTIS Pheno VE30A and VE40A Imaging SystemSiemens is recalling ARTIS Pheno VE30A and VE40A imaging systems (Model 10849000) due to unregulated dose causing unintentional low-dose radiation exposure.
FDA•MODERATEMesh Style Tip ProtectorsHealthmark Industries is recalling Mesh Style Tip Protectors (models CSW-03-2.0 and CSW-04-4.0) due to a lack of FDA clearance.
FDA•MODERATELinkBio CORE WorkstationLinkBio CORE Workstation (87-9136) may display incorrect Planning Date on Start Case menu.
FDA•MODERATEiLet Bionic PancreasBeta Bionics is recalling iLet Bionic Pancreas (software 1.4.2–1.4.3) for Dexcom G7 compatibility issues that may disable glucose correction dosing.
FDA•LOWYunker Energy & Health Herbal SupplementSato Pharmaceutical is recalling Yunker Energy & Health Herbal Supplement because it does not meet label claims for Vitamin E content.
FDA•MODERATETETAS Mireya Cherry Milkshake PopsicleASUKAR FOODS CORP is recalling TETAS Mireya Cherry Milkshake popsicles (UPC 83822654822) due to undeclared soy lecithin.
FDA•MODERATE0.9% Sodium Chloride Injection, USPFresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP, 250 mL bags due to a lack of assurance of sterility.
14 products
NHTSA•MODERATEATC PL700 and PL750 Recreational TrailersATC is recalling 2023–2026 PL700 and PL750 trailers over carbon monoxide entering the cabin from generator exhaust.
NHTSA•MODERATEMack TerraPro Engine Control Unit SoftwareMack is recalling 2022–2027 TerraPro trucks; ECU software may allow engine start in gear, risking unexpected movement.
NHTSA•MODERATEVolkswagen Jetta Transmission Ground WireVolkswagen is recalling 2025–2026 Jetta vehicles over loose transmission ground wire fire risk.
NHTSA•MODERATEVolvo EX30 Seat Belt Warning SystemVolvo is recalling 2025–2026 EX30 and 2026 EX30CC vehicles over a faulty seat belt warning chime system.
NHTSA•MODERATEARBOC Spirit of Freedom/Mobility Rear ABS SystemARBOC is recalling 2018–2026 Spirit of Freedom/Mobility buses over rear ABS malfunction that increases crash risk.
FDA•MODERATEB Braun Infusion Pump Administration SetsWindstone Medical Packaging is recalling Pre Op Kits containing B Braun IV administration sets due to potential medication backflow or priming issues.
3 products
FDA•MODERATEMedtronic Sphere-9 Cardiac Ablation CatheterMedtronic Sphere-9 Catheter (Model AFR-00001) may cause ventricular fibrillation in patients with Biotronik ICDs or CRT-Ds during radiofrequency ablation therapy.
FDA•MODERATEArrow Echogenic Introducer NeedleArrow is recalling the Echogenic Introducer Needle due to a manufacturing error involving the device's liquid adhesive.
13 products
FDA•MODERATEHorizon Organic Chocolate Lowfat MilkHorizon Organic is recalling chocolate lowfat milk in 8-oz cartons due to compromised package integrity.
FDA•MODERATEARTIS pheno and ARTIS Icono Biplane X-ray SystemSiemens is recalling ARTIS pheno and ARTIS Icono X-ray systems (Models 10849000, 11327600, 11328100, 11327700) due to erroneous dose display during patient exams.
FDA•MODERATEArjo Tenor Mobile Patient LiftArjo Tenor patient lifts (Models KHA1000 US, KHA1010 US) recalled for actuator failure risk causing sudden arm drop.
FDA•MODERATEPan de Bono Cheese BreadSouth Florida Food recalling Pan de Bono Cheese Bread (14.4 lb boxes) due to undeclared soy.
FDA•MODERATEIcosapent Ethyl Capsules, 1 gramZydus Pharmaceuticals is recalling Icosapent Ethyl Capsules (NDC 70710-1592-7) due to oxidized ingredient causing red dots and melted capsules.
FDA•MODERATEnanOss 3D Advanced Bone Graft SubstituteXTANT Medical is recalling nanOss 3D bone graft substitutes due to an incorrect five-year shelf life label instead of the validated four years.
FDA•MODERATEMilestone Vacuum Bag SU Large Specimen ContainerMilestone is recalling Vacuum Bag SU Large specimen containers (Model 68409SS) due to possible reagent leakage.
FDA•MODERATELSL Healthcare Central Line Dressing KitLSL Healthcare is recalling Central Line Dressing Kits (Model 2717H) due to the inclusion of non-sterile alcohol prep pads.
6 products
FDA•MODERATEKiwi Omni Vacuum Delivery SystemClinical Innovations is recalling the Kiwi Omni Vacuum Delivery System (Model VAC-6000MT) due to a risk of device breakage during use.
FDA•MODERATESiemens ARTIS pheno X-Ray SystemSiemens is recalling the ARTIS pheno x-ray system (Model 10849000) because it may incorrectly display an x-ray dose of zero during use.
2 products
FDA•MODERATEPhilips Spectral CT on RailsPhilips Spectral CT on Rails (Model 728334) requires a software update to address gantry positioning, message display, and menu option issues.
NHTSA•MODERATEMercedes-Benz GLA 250 Door CableMercedes-Benz is recalling 2026 GLA 250 vehicles over an incorrectly installed door cable that may prevent opening from inside.
NHTSA•MODERATEPebble Flow Recreational Trailer Solar PanelPebble is recalling 2026 Flow trailers; solar panels may detach due to adhesive failure.
NHTSA•MODERATEKia Telluride and K4 Seat Belt BuckleKia is recalling 2027 Telluride and 2026 K4 vehicles over rear seat belt buckles that may not latch properly.
FDA•MODERATEUvlizer Handheld UV-C Germicidal WandUvlizer UV-C germicidal wands can expose users to unsafe UV-C radiation levels above international safety guidelines.
- FDA•MODERATEUvlizer Handheld UV-C Germicidal Wand
Uvlizer UV-C germicidal wands may expose users to unsafe UVC radiation levels above international safety guidelines.
FDA•MODERATESemaglutide-Glycine-Cyanocobalamin InjectableNorthwest Compounders is recalling Semaglutide-Glycine-Cyanocobalamin Injectable vials due to lack of assurance of sterility.
FDA•MODERATECUSA Clarity C7000 ConsoleIntegra LifeSciences is recalling CUSA Clarity C7000 Console (Software 2.1.1.909) due to unresponsive touch screen.
CPSC•Tomum Minoxidil Hair Growth Treatment Spray BottlesBelleka is recalling Tomum Minoxidil Hair Growth Treatment (100 mL) spray bottles due to lack of child-resistant packaging.
CPSC•Cubimana Island Storm 3 In 1 Building SetsCubimana Island Storm 3 In 1 Building Sets (Model HG1004) recalled for accessible button cell batteries posing serious injury risk to children.
CPSC•Forever 21 Kids Disney Mickey Mouse Pajama PantsForever 21 is recalling Disney Mickey Mouse Pajama Pants (item 01334347) in sizes 5/6–13/14 due to flammability standard violations and burn hazard.
CPSC•HALO Magic SleepsuitHALO Magic Sleepsuit (batch codes PO30592, PO30641, PO30685) recalled due to detachable zipper head choking hazard.
FDA•MODERATEVegetable DumplingsJFE Franchising is recalling Vegetable Dumplings over potential glass contamination.
7 products
FDA•MODERATEBrimonidine Tartrate/Timolol Maleate Ophthalmic SolutionApotex is recalling Brimonidine Tartrate/Timolol Maleate eye drops (NDC 60505-0589-1) due to lack of sterility assurance.
FDA•MODERATECook Medical Arterial Pressure Monitoring TrayCook Medical is recalling Arterial Pressure Monitoring Trays because the labeled expiration dates exceed the device's actual shelf life.
19 products
FDA•MODERATETornier HRS Max Tuberosity Bodies and TrialsTornier is recalling mislabeled shoulder replacement components that are incompatible with the HRS Max system.
FDA•MODERATEVue Motion V12 Imaging SystemPhilips Vue Motion V12 (1017979) may display image frames out of sequence during dynamic imaging runs.
NHTSA•MODERATEForest River Impression Fifth Wheel WiringForest River is recalling 2026 Impression fifth wheel trailers with improperly stripped wires that may cause electrical arcing and fire.
NHTSA•MODERATEDynamax Europa and Grand Sport GT Electrical Distribution PanelForest River is recalling 2026 Dynamax Europa and Grand Sport GT motorhomes over improper electrical distribution panel grounding that may cause electrocution risk.
NHTSA•MODERATEWebasto CV Standard Gen1 High Voltage BatteryWebasto is recalling CV Standard Gen1 Batteries (part nos. 5613175, 5610618, 5610610) over potential failure causing crash or fire risk.
NHTSA•MODERATEGeneral Motors Express and Savana Cutaway TiresGM recalls 2025–2026 Express and Savana Cutaway vehicles with damaged tire sidewalls that may cause sudden air loss.