All Recalls

K.Z. is recalling 2026 Durango trailers with Curt Touring Coil Suspensions due to incorrectly tightened shock bolts that may detach.

Volkswagen is recalling 2024 Tiguan vehicles because a software error may cause the rearview camera to fail to display at startup.

Wabash is recalling 2019-2027 Platform trailers because missing conspicuity tape may reduce visibility and increase crash risk.

Haleon is recalling Gas-X Simethicone 125 mg SoftGels (120 count), UPC 3 00674 35041 9, due to incomplete inactive ingredient labeling.

Wellnov recalls liquid multivitamins and supplements over cGMP deviations risking bacterial contamination and C. botulinum.

Lupin is recalling Liraglutide Injection (NDC 70748-346-02 and 70748-346-03) due to white thread-like particulate matter in the cartridge.

Hyundai is recalling 2025-2026 Santa Cruz and Tucson vehicles because a software error may cause the brakes to apply unexpectedly.

Tesla is recalling 2025-2026 Model Y vehicles that may be missing a required certification label, posing a risk of vehicle overloading.

Hyundai is recalling 2025 Ioniq 5 and 2026 Ioniq 9 vehicles due to a risk of rear suspension fasteners loosening and causing loss of control.

Jerr-Dan is recalling XLP Carrier kits due to non-compliant reverse and brake light assemblies that may increase the risk of a crash.

American Health Packaging recalls Primidone Tablets 250 mg due to trace Acemetacin contamination.

Sagent Pharmaceuticals is recalling Busulfan Injection (NDC 25021-241-10) due to failed impurities and degradation specifications.

Primidone 50 mg tablets recalled due to possible cross-contamination with Acemetacin.

Lannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.

ICU Medical is recalling Oncology Extension Set REF: CL3960 due to a potential leak that could cause therapy interruption or hazardous exposure.

Keystone is recalling 2024-2026 Cougar, Alpine, Montana, and Walkabout trailers (NHTSA 26V313000) due to incorrectly tightened shock bolts.

Endera is recalling 2025-2026 Shuttle transit buses because wheelchair restraint retractors may fail to lock, increasing injury risks.

Oshkosh is recalling 2025 NGDV electric vehicles due to a battery contactor failure that may cause a sudden loss of drive power.

PS Seasoning recalls Ellsworth Sour Cream + Onion Seasoning and other seasonings over Salmonella risk.

Tangent Endoscopy is recalling single-use digital catheters due to potential fractures at the distal shaft tip.

Becton, Dickinson and Company is recalling multiple variants of its Swan-Ganz pulmonary artery catheters due to a potential risk of valve leakage that may affect the balloon inflation performance.

Hyundai is recalling 2024-2026 Elantra Hybrid vehicles because the hybrid power control unit may overheat, increasing the risk of fire.

Hyundai is recalling 2015-2016 Elantra and 2016 Elantra GT vehicles because the driver's air bag inflator may rupture during deployment.

Altec is recalling various aerial device vehicles because the emergency stop may fail to halt hydraulic functions, increasing injury risk.

Cosyland is recalling children's tower stools (models CS0003 and CS0092-4) due to collapse, fall, and entrapment hazards.

Generac and DR Power pressure washers are recalled due to a carbon monoxide poisoning risk from a malfunctioning electric start button.

Guidecraft is recalling children's standing towers due to a fall hazard caused by a platform that can loosen and detach.

LiCB CR2032 lithium coin batteries are recalled for lacking child-resistant packaging and warning labels, posing a severe ingestion hazard.

Misco Sports badminton toy sets are recalled due to a battery ingestion hazard from easily accessible button cell batteries in the shuttlecock.

Petzl is recalling SIMBA and SWAN EASYFIT harnesses due to a buckle defect that poses a serious fall hazard.

Superbobi pool drain covers are recalled for failing to meet safety standards, posing entrapment and drowning hazards to swimmers.

Tiyol pull string teething toys (Model 688-59) are recalled due to a choking hazard from strings that can lodge in a child's throat.

Zwilling is recalling Enfinigy electric kettles because the handle can detach, posing a burn hazard from hot contents.

Honda is recalling 2024-2025 Honda Prologue and 2024 Acura ZDX vehicles because the rearview camera may display a distorted or blank image.

BMW is recalling 2017-2018 C Evolution motorcycles due to a fire risk from potential corrosion in the DC/DC converter electrical connection.

GM is recalling 2025–2026 Cadillac, Chevrolet, and GMC vehicles with 24-inch wheels due to incorrect front wheel hub bolts that may loosen.

Sun Pharma recalls DOXOrubicin Liposome Injection 50 mg/25 mL vials due to glass particulate matter.

Integra LifeSciences is recalling the Codman CerebroFlo EVD Catheter due to out-of-specification endotoxin results.

Arrow Edge hemodialysis catheterization product recalled: sheath introducer may not split, risking injury.

BARD Dynamic Deca Steerable EP catheter recalled due to incomplete seals on sterile product.

Edwards Lifesciences is updating the labeling for the EVOQUE tricuspid delivery system to include a warning about potential functionality issues.

Hale Products is recalling Weldon UV800 display units (part numbers 610-00060-080-51, 610-00060-080-50, 610-00060-081, 610-00091) due to failure.

Hiab is recalling Waltco MDV series liftgates because broken deck pins may cause the platform to fall, posing an injury risk.

Lucid is recalling 2024-2025 Air vehicles due to a Gen 4 inverter defect that may cause a loss of drive power and increase crash risk.

Fly By Jing recalls Creamy Sesame Noodles over possible undeclared peanut allergen.

ZYMUTEST HIA IgG ELISA kit lot FD1265 distributed with outdated flyer containing incorrect positive control values.

Philips is recalling Azurion imaging systems due to potential loosening or breakage of Cable Hose Carrier bolts and plastic parts.

Quidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.

Stryker is recalling the FluidSmart Urology Tube Set (REF LL0006) due to the distribution of nonconforming products.

Hologic recalls Selenia Dimensions mammography systems over loose or broken internal bolts.