NHTSA•MODERATE
Ford Bronco Transmission-Transfer Case Joint
Ford is recalling 2021–2025 Bronco vehicles for transmission-transfer case misalignment that may cause loss of drive power or rollaway.
Filters
Category
Agency
Severity
All Recalls
Back to home ←
NHTSA•MODERATEFord Ranger Sun Visor Wiring HarnessFord is recalling 2024–2026 Ranger vehicles over sun visor wiring that may short and cause fire.
FDA•MODERATEPhilips Achieva and MR 7700 MR Elastography SystemsPhilips is recalling MR Elastography systems (models 782130, 781196, 781296) due to a software error that can cause inaccurate stiffness values.
19 products
FDA•MODERATESpecially SELECTED Vanilla Creme BruleeLactalis Canada is recalling Specially SELECTED Vanilla Creme Brulee (3.6 oz) over possible glass contamination.
FDA•MODERATEDexcom G7 CGM iOS AppDexcom is recalling G7 CGM iOS app versions 2.9.0–2.11.2 due to a software defect that may delay glucose alerts and readings.
4 products
NHTSA•MODERATEEntegra Ethos Seating Capacity LabelJayco is recalling 2025–2026 Entegra Ethos RVs with incorrect seating capacity labels that may result in unbelted passengers.
NHTSA•MODERATEHarley-Davidson Softail Rear Brake LineHarley-Davidson is recalling 2025–2026 Softail motorcycles (FLHC, FXBB, FXLRS, FXLRST) due to rear brake line contact with the BCM causing brake failure.
FDA•MODERATE52USA Strawberry Popping Boba52USA Strawberry Popping Boba is recalled for containing unapproved food colors including FD&C Yellow 5, Yellow 6, and Red 40.
6 products
FDA•MODERATEPhysio-Control LIFEPAK DefibrillatorsPhysio-Control is recalling various LIFEPAK defibrillators due to missing performance inspection documentation that may impact device therapy.
FDA•MODERATELUCAS Chest Compression SystemJolife AB is recalling LUCAS 2, 3, and 3.1 chest compression systems due to missing service documentation.
2 products
FDA•MODERATESwad Orange Flavored Masala CandySwad Orange Flavored Masala Candy is being recalled due to the presence of undeclared FD&C Yellow 6.
2 products
FDA•MODERATEHalyard Purezero Ultraviolet Nitrile Exam GlovesHalyard is recalling Purezero Ultraviolet Nitrile Exam Gloves due to a failure to meet chemical permeation performance specifications.
NHTSA•MODERATEKia Carnival Fuel Pipe ConnectionKia is recalling 2022–2026 Carnival vehicles for fuel leak risk at the fuel pipe connection.
NHTSA•MODERATEGenesis Fuel Pipe ConnectionGenesis is recalling GV70, G90, G80, and GV80 models over fuel leak risk at pipe connection.
NHTSA•MODERATE2026 Bentley Bentayga Tire Placard LabelBentley is recalling 2026 Bentayga vehicles with incorrect tire placard weight capacity labels.
NHTSA•MODERATENissan Cube Driver Air Bag InflatorNissan is recalling 2009–2010 Cube vehicles; driver air bag inflator may detach during deployment.
FDA•MODERATECodman CerebroFlo EVD CatheterIntegra LifeSciences is recalling the CerebroFlo EVD Catheter due to out-of-specification endotoxin results.
FDA•MODERATEBard Dynamic Deca Steerable Electrophysiology CatheterStryker is recalling the Bard Dynamic Deca Steerable Electrophysiology Catheter due to incomplete sterile packaging seals.
26 products
FDA•MODERATEMedline Eye Tray-LF Convenience KitMedline is recalling Eye Tray-LF kits containing mislabeled Cardinal Health syringes that may lead to incorrect insulin dosing.
FSIS•MODERATEQuality Meat Sky Ranch Marinated Beef and Pork ProductsSky Ranch Meat recalled marinated beef and pork products (1.5-lb containers, Dec 2025–Apr 2026) for undeclared sesame allergen.
4 products
NHTSA•MODERATEHonda Odyssey Side Air BagsHonda is recalling 2018–2022 Odyssey vehicles; side air bags may deploy unexpectedly due to software error.
NHTSA•MODERATEJeep Cherokee Brake System Control ModuleChrysler is recalling 2026 Jeep Cherokee vehicles for brake module failure that disables ABS and electronic stability control.
NHTSA•MODERATEThomas Built Saf-T-Liner C2 Warning Lights and Stop SignThomas Built Saf-T-Liner C2 school buses (2024–2027) may lose warning lights and stop sign due to door switch software defect.
NHTSA•MODERATEIC Bus EVSB School Bus High Voltage Disconnect SwitchInternational is recalling 2022–2027 IC Bus EVSB school buses; high voltage disconnect switch may fail to cut power.
NHTSA•MODERATEJeep Wrangler Child Seat Tether WeldsChrysler is recalling 2026 Jeep Wrangler vehicles over insufficient child seat tether welds that may reduce crash restraint.
NHTSA•MODERATENova Bus Ricon Hidden Frame WindowsNova Bus is recalling Ricon hidden frame windows due to inadequate adhesion that may cause glass detachment during a crash.
NHTSA•MODERATERam 1500/2500/3500/4500/5500 Instrument Panel DisplayChrysler is recalling 2025–2026 Ram 1500/2500/3500/4500/5500 vehicles over instrument panel display failure that hides critical safety information.
NHTSA•MODERATEEnovation Controls PowerView 700 DisplayAkron Brass is recalling PowerView 700 displays (part numbers 610-00060-080-ST/080) that may fail to power on, preventing activation of emergency lights and equipment.
FDA•MODERATEOmega-3-Acid Ethyl Esters Capsules 1 gramMajor Pharmaceuticals is recalling Omega-3-Acid Ethyl Esters Capsules 1 gram (NDC 0904-7495-06) due to failed capsule shell specifications.
FDA•MODERATEThermedx FluidSmart Urology Tube SetStryker is recalling the FluidSmart Urology Tube Set due to the distribution of nonconforming products.
NHTSA•MODERATELexus RC, GS, IS Fuel PumpToyota is recalling 2015–2022 Lexus RC, 2016–2020 GS, and 2022 IS vehicles over fuel pump failure risk.
NHTSA•MODERATEForest River Westbrook and Avenger Travel TrailersForest River is recalling 2026 Westbrook and Avenger travel trailers with incorrect dry weight labels that may cause overloading and crash risk.
FDA•MODERATEDesmopressin Nasal Spray, USP 10 mcg/0.1 mLApotex is recalling Desmopressin Nasal Spray (NDC 60505-0815-0) due to defective bottle caps with missing or dislodged liners.
3 products
FDA•MODERATESelenia Dimensions Mammography SystemsHologic is recalling 15+ models of Selenia Dimensions Mammography Systems due to a risk of loose, missing, or broken internal bolts.
2 products- Device RecallFDA•MODERATEMedtronic SynchroMed Flex Infusion Mode A810 Software
Medtronic is recalling A810 software for SynchroMed pumps due to a display error that can cause incorrect or failed infusion delivery.
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
FSIS•MODERATEWalmart Great Value Dino Shaped Chicken Nuggets — RetractionFSIS retracts alert for Walmart Great Value Dino Nuggets (Feb 10 2027) after confirming no lead contamination.
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 is recalling Original Spreadable Spun Honey due to potential contamination with stainless steel or plastic foreign objects.
5 products