FDA•MODERATE
Hologic Selenia Dimensions Mammography Systems
Hologic is recalling 15+ models of Selenia Dimensions Mammography Systems due to potential internal bolt failure.
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Back to home ←- Device RecallFDA•MODERATEMedtronic SynchroMed Flex Infusion Mode A810 App
Medtronic is recalling the A810 software app for SynchroMed pumps due to a display error that can disrupt the programmed infusion schedule.
2 products 
FDA•MODERATESwan-Ganz CathetersBecton, Dickinson and Company is recalling 15+ models of Swan-Ganz Catheters due to a risk of hub leakage or breakage.
3 products
NHTSA•MODERATECan-Am Origin Electric Motorcycle Front Brake CaliperBRP is recalling 2025 Can-Am Origin electric motorcycles for front brake caliper failure risk.
FDA•MODERATEBulk Horchata PowderMarquez Brothers International is recalling Bulk Horchata Powder due to undeclared milk, which poses a risk to those with milk allergies.
3 products
FDA•MODERATEAlendronate Sodium Oral Solution 70 mg/75 mLHikma is recalling Alendronate Sodium Oral Solution 70 mg/75 mL (NDC 0054-0282-59) due to out-of-specification assay results.
FDA•MODERATEBD GasPak EZ Gas Generating Pouch SystemsBecton Dickinson is recalling BD GasPak EZ CO2 and Campy Gas Generating Pouch Systems due to insufficient carbon dioxide production.
2 products
NHTSA•MODERATEGreenpower Nano Beast and Beast School Bus Cross View MirrorGreenpower is recalling 2020–2024 Nano Beast and 2021–2024 Beast school buses with missing Cross View Mirror warning labels, risking driver misuse and crashes.
NHTSA•MODERATEPierce Arrow XT/Enforcer/Impel/Velocity Firm-On-Ground LightPierce is recalling 2015–2026 Arrow XT/Enforcer/Impel/Velocity aerial firetrucks; firm-on-ground light may fail to deactivate when stabilizer loses ground contact.
NHTSA•MODERATEHyundai Ioniq 6, Genesis G90, Santa Fe Seat Belt AnchorsHyundai is recalling Ioniq 6, Genesis G90, and Santa Fe vehicles over detachable seat belt anchors that may fail to restrain occupants.
FDA•MODERATEClaravis (isotretinoin capsule, USP) 10 mgTeva is recalling Claravis 10 mg capsules (NDC 0555-1054-56, 0555-1054-86) due to out-of-specification Tretinoin impurity levels.
3 products
FDA•MODERATEDelflex Peritoneal Dialysis SolutionFresenius Medical Care is recalling Delflex Peritoneal Dialysis Solution due to potential bag leaks and a lack of sterility assurance.
2 products
FDA•MODERATEQuickVue Dipstick Strep A TestQuidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
FDA•MODERATELVIS Intraluminal Support DeviceMicroVention recalls LVIS Intraluminal Support Devices (REF 214022-CAS, 214518-CAS, 213517-CAS) due to dimensional nonconformance risking vessel injury or thrombosis.
FDA•MODERATELiquid Blenz Soursop BittersLiquid Blenz Soursop Bitters are recalled due to potential Clostridium botulinum contamination and unauthorized health claims.
13 products
FDA•MODERATEDakota Honey Company Spreadable Spun HoneyDakota Honey Company is recalling Original Spreadable Spun Honey due to potential contamination with stainless steel or plastic foreign objects.
5 products
NHTSA•MODERATEMercedes-Benz Drive Shaft Universal JointMercedes-Benz is recalling certain 2018–2020 E-Class and Maybach models due to drive shaft universal joint breakage risk.
NHTSA•MODERATEAutocar ACX Xpeditor Winter Front CoverAutocar recalls 2025–2026 ACX Xpeditor vehicles; winter front cover may disable forward collision warning system.
NHTSA•MODERATEGraco SnugRide Turn & Slide Infant Car SeatGraco SnugRide Turn & Slide infant car seats may detach from the base in a crash, posing injury risk.
2 products
FDA•MODERATEDePuy Synthes Attune Revision Hinge Femoral ComponentDePuy Synthes is recalling the Attune Revision Hinge Femoral component due to a potential loss of sterility from packaging defects.
9 products
FDA•MODERATEFain's Blackberry Honey SpreadWalker Honey Co. is recalling Fain's Blackberry Honey Spread due to potential stainless steel or plastic particle contamination.
10 products
FDA•MODERATELundberg Family Farms Jasmine White RiceLundberg Family Farms is recalling 32 oz Jasmine White Rice due to potential foreign material contamination.
FDA•MODERATEGrace Medical Stapes ProsthesisGrace Medical is recalling the Titanium/Fluoroplastic Piston Stapes Prosthesis due to incorrect functional length listed on the labeling.
CPSC•Coluans Christmas Light-Up RingsColuans Christmas Light-Up Rings (model SJP-50) recalled for accessible button cell batteries posing serious ingestion hazard to children.
CPSC•Beestech Spiral Children's Tower ToyBeestech spiral tower toy (model Bee-210316-01) recalled for choking hazard; violates small ball ban for children under 3.
CPSC•Granitestone Diamond Pro Blue Stainless Sauté PansE Mishan recalls Granitestone Diamond Pro Blue sauté pan sets (UPC 0-80313-08131-6) due to detachable metal cap that can eject when heated, causing impact and burn hazards.
CPSC•TecFlox Minoxidil Topical Solution BottlesTecFlox is recalling Minoxidil Topical Solution bottles lacking child-resistant packaging, posing poisoning risk to children.
CPSC•HTRC and Haisito T400 Battery ChargersHTRC and Haisito T400 battery chargers can ignite, posing a fire hazard and risk of serious injury or death.
CPSC•ELENKER Portable Bed RailsELENKER portable bed rails (models HFK-5115, HFK-5116, HFK-5124) recalled for entrapment and asphyxiation risk; lack required safety labels.
CPSC•Ocun Condor HMS Triple CarabinerOcun is recalling Condor HMS Triple Carabiners (batches 24003xx–25006xx) due to gate malfunction risk causing falls.
CPSC•Universal Broadmoor Canopy Bed FramesSamson International recalls Universal Broadmoor canopy bed frames (models M24109230, M24109240, M24107230, M24107240) due to collapsing canopy beams.
CPSC•Member's Mark Children's Pajama SetsSam's Club recalls Member's Mark children's pajama sets (sizes XS–XL) for violating flammability standards and posing burn hazard.
CPSC•Tuymec Minoxidil Hair Growth Spray BottlesTuymec Minoxidil Hair Growth spray bottles lack required child-resistant packaging, posing poisoning risk to children.
CPSC•Gavoyeat Halloween Light-Up RingsGavoyeat Halloween Light-Up Rings recalled for accessible button cell batteries posing serious ingestion hazard to children.
CPSC•Sangohe Adult Portable Bed RailsSangohe bed rails models 504E and 504Q recalled for entrapment and asphyxiation risk; sold on Amazon August 2023–February 2026.
FDA•MODERATEReadyMeals Turkey Bacon & Cheddar Pretzel Duo SandwichReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich is recalled due to undeclared sesame.
NHTSA•MODERATEBMW K 1600 and Grand America Reverse Gear Control UnitBMW is recalling 2017–2025 K 1600 GT/GTL/B and 2018–2025 Grand America motorcycles over reverse gear control unit overheating and fire risk.
NHTSA•MODERATEChevrolet Malibu Rearview CameraGM recalls 2023–2025 Chevrolet Malibu rearview cameras that may display distorted or blank images.
NHTSA•MODERATEChevrolet Corvette Rear Turn Signal Warning SystemGM is recalling 2025–2026 Chevrolet Corvette models over a software error that may prevent detection of rear turn signal failure.
NHTSA•MODERATEKeystone Montana Fifth Wheel UnderbellyKeystone is recalling 2026 Montana fifth wheel trailers; underbelly may detach during transit, creating road hazard.
FDA•MODERATESterile Water for Injection USPB. Braun is recalling 3000 mL Sterile Water for Injection USP bags distributed nationwide due to potential sterility and leakage issues.
4 products
FDA•MODERATELidocaine HCl Injection 1% 5 mL VialsHuons is recalling Lidocaine HCl injection 1% 5 mL vials due to a lack of assurance of sterility.
9 products
FDA•MODERATEepoc BGEM BUN Test CardSiemens is recalling epoc BGEM BUN Test Cards due to the risk of inaccurate pH and carbon dioxide results that may lead to improper treatment.
FDA•MODERATEPhilips Bridge Prep KitMerit Medical Systems is recalling the Philips Bridge Prep Kit due to potential catheter resistance during use.
4 products
FDA•MODERATEda Vinci X and Xi Surgical System Universal Surgical ManipulatorIntuitive Surgical is recalling USM arm sub-assemblies for da Vinci X and Xi systems due to a risk of internal screw breakage.
2 products
FDA•MODERATEOne Step 10A In Vitro Diagnostic TestDFI is recalling the One Step 10A in vitro diagnostic test because it was distributed without required FDA premarket clearance or approval.
7 products
NHTSA•MODERATEVolvo VNL and VNR Turn Signal SystemVolvo is recalling 2025–2027 VNL and 2026–2027 VNR trucks over turn signal failure risk.
NHTSA•MODERATEAudi 2026 Q3 Sunroof SystemAudi is recalling 2026 Q3 vehicles for sunroof software that allows remote closing without operator visibility.
NHTSA•MODERATEChevrolet Low Cab Forward and Isuzu NRR Wire HarnessIsuzu is recalling 2025–2027 Chevrolet Low Cab Forward and Isuzu NRR vehicles over improperly secured wire harnesses that may chafe, causing engine stall, brake failure, or fire.
NHTSA•MODERATEMack Pioneer and Anthem Trailers Turn SignalMack is recalling 2025–2027 Pioneer and 2027 Anthem trailers with non-functional turn signals that increase crash risk.