FDA•MODERATE
Arjo Tenor Mobile Patient Lift
Arjo Tenor patient lifts (Models KHA1000 US, KHA1010 US) recalled for actuator failure risk causing sudden arm drop.
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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.
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 due to incorrect expiration date labeling that exceeds the product's 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.
NHTSA•MODERATEChevrolet Silverado 3500 and GMC Sierra 3500 Fuel PumpGM recalls 2025–2026 Silverado 3500 and Sierra 3500 dual-tank models for fuel pump failure risk causing engine stall.
NHTSA•MODERATEMitsubishi Fuso Rizon Electrical Control UnitMitsubishi Fuso is recalling 2024–2025 Rizon trucks (FEC7K, FEC9K, FECXK) for electrical control unit errors that may prevent driving.
NHTSA•MODERATEToyota Highlander Second-Row Seat Back LatchToyota is recalling 2021–2024 Highlander and Highlander Hybrid vehicles over second-row seat back latch failure.
FDA•MODERATEBiDop 3 Pocket DopplerKoven Technology is recalling the BiDop 3 Pocket Doppler because its labeling includes an uncleared fetal indication for use.
2 products
NHTSA•MODERATEKumho Solus TA11 TireKumho is recalling Solus TA11 tires (225/60R16) due to potential tread separation and crash risk.
NHTSA•MODERATEAudi Q8, A7, A6 Lane Departure Warning SystemAudi is recalling 2019 Q8, A7, A6 vehicles; lane departure warning may be deactivated due to software error.
FDA•MODERATEMontebianco Base VeganDisaronno is recalling Montebianco Base Vegan (SKU 113542) due to undeclared milk allergen exceeding safe levels.
FDA•MODERATEAjinomoto Vegetable & Edamame DumplingsAjinomoto is recalling Green Gyoza Vegetable & Edamame Dumplings due to potential glass fragment contamination.
11 products
FDA•MODERATETemozolomide Capsules 5mgRising Pharmaceuticals is recalling Temozolomide Capsules 5mg (NDC 16571-816-51) due to failed impurities and degradation specifications.
FDA•MODERATEArtificial Tears Sterile Lubricant Eye DropsK.C. Pharmaceuticals is recalling various brands of Artificial Tears eye drops nationwide due to a lack of assurance of sterility.
15 products
FDA•MODERATEPhilips Allura Xper FD20 Biplane X-Ray SystemPhilips is recalling Allura Xper FD20 Biplane X-ray systems due to potential foot switch failure causing intermittent or no imaging.
22 products
FDA•MODERATEOXOID Microbact 12L Listeria Identification KitOxoid is recalling Microbact 12L Listeria Kit (MB1128A, Lot 4494873) due to risk of incorrect organism identification from ambiguous color reactions.
NHTSA•MODERATEFord EGR ValveFord is recalling 2025 Ranger, Nautilus, Mustang, Maverick, Explorer, Escape, Corsair, Bronco Sport, and Bronco vehicles over EGR valve failure causing loss of drive power.
NHTSA•MODERATEFord Bronco and Edge Accessory Protocol Interface ModuleFord is recalling 2021–2026 Bronco and 2021–2024 Edge vehicles; APIM overheating may disable rearview camera display.
NHTSA•MODERATEFord Escape, Corsair, Aviator, Explorer Rearview CameraFord is recalling Escape, Corsair, Aviator, and Explorer vehicles (2020–2024) for inverted rearview camera images that reduce rear visibility.
NHTSA•MODERATEFord Explorer Passenger-Side HeadlightFord is recalling 2025–2026 Explorer vehicles; passenger-side headlight may turn incorrectly in curves, increasing crash risk.
NHTSA•MODERATEFord Explorer, Escape, Aviator, Corsair Windshield Wiper MotorFord is recalling 2020–2022 Explorer, Escape, Aviator, and Corsair vehicles for windshield wiper motor failure that may reduce visibility.
NHTSA•MODERATEFord F-250 SD and F-350 SD DriveshaftFord is recalling 2026–2025 F-250 SD and F-350 SD vehicles over driveshaft separation risk.
NHTSA•MODERATEFord E-350 and E-450 Backup Alarm ConnectorFord is recalling 2026–2027 E-350 and E-450 vehicles; backup alarm connector may detach, silencing the reversing alert.
NHTSA•MODERATELincoln Navigator Driver's SeatFord is recalling 2026 Lincoln Navigator vehicles due to driver's seat reversing unexpectedly at low speeds.
FDA•MODERATEFarmhouse Fresh Midnight Clearing Night LotionFarmhouse Fresh is recalling Midnight Clearing Night Lotion acne treatment due to benzene contamination.
4 products