NHTSA•MODERATE
Mack TerraPro Engine Control Unit Software
Mack is recalling 2022–2027 TerraPro trucks; ECU software may allow engine start in gear, risking unexpected movement.
Filters
Category
Agency
Severity
All Recalls
Back to home ←
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 IV Administration SetsWindstone Medical is correcting B Braun IV administration sets due to potential medication backflow and priming occlusion risks.
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 International is recalling the Echogenic Introducer Needle due to a supplier notice regarding incorrectly manufactured liquid adhesive.
13 products
FDA•CRITICALIntuitive SureForm 30 Gray ReloadsIntuitive Surgical is recalling SureForm 30 Gray Reloads (Ref 48230M-05, 48230M-06) due to the risk of an incomplete staple line.
FDA•CRITICALCostco Service Deli Meatloaf SeasoningGriffith Foods is recalling Costco Service Deli Meatloaf Seasoning due to potential Salmonella contamination.
3 products
FDA•MODERATEHorizon Organic Chocolate Lowfat MilkHorizon Organic is recalling chocolate lowfat milk in 8-oz cartons due to compromised package integrity.
FDA•CRITICALNuts.com Espresso Malted Milk BallsNuts.com is recalling Espresso Malted Milk Balls due to undeclared wheat and soy allergens.
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.
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.
FDA•CRITICALMID EAST Jordanian Zaatar Spice MixKradjian Importing Company is recalling MID EAST Jordanian Zaatar spice mix due to undeclared sesame and wheat allergens.
FDA•CRITICALGorditas and DoraditasDistribuidora de Alimentos Sendero is recalling Gorditas and Doraditas due to undeclared wheat and soy allergens.
2 products
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•CRITICALEscape Trailer Recreational Trailer Spare Tire CarrierEscape Trailer recalls 2025 E17, E19, E21, E5.0 trailers; spare tire carrier may detach due to welding defect.
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.