
NHTSA•MODERATE
Harley-Davidson Softail Rear Brake Line
Harley-Davidson is recalling 2025–2026 Softail motorcycles (FLHC, FXBB, FXLRS, FXLRST) due to rear brake line contact with the BCM causing brake failure.

Harley-Davidson is recalling 2025–2026 Softail motorcycles (FLHC, FXBB, FXLRS, FXLRST) due to rear brake line contact with the BCM causing brake failure.

Taro recalls Fluocinonide 0.05% Cream 15g tubes due to out-of-spec viscosity.
3 products
Wilson-Cook Medical is recalling the Instinct Plus Endoscopic Clipping Device due to a potential for the device to malfunction.

Head is recalling various ski boot models with fluorescent yellow components due to a fall hazard from potential material deterioration.

Besslly Halloween Pumpkin Carving Kits (Model CHD-014-2) are recalled due to a serious battery ingestion and chemical burn hazard.

Prestige is recalling Supernova and Typhoon butane lighters because they lack required child-resistant mechanisms, posing fire and burn risks.

Happiness Light LED lights are recalled due to a serious battery ingestion hazard that can cause severe internal chemical burns and death.

Muscccm pool drain covers are recalled due to entrapment and drowning hazards for failing to meet federal safety standards.

Member's Mark 7' Pre-Lit Twinkling Buck is recalled due to a burn hazard caused by an overheating resistor.

Shenzhen Shijingjie is recalling male-to-male extension cords (models RY-US-06 and RY_US-1.5) due to electrocution, fire, and CO poisoning risks.

ShymeryDirect LED lights are recalled due to a serious battery ingestion hazard and missing safety warnings.

Yeeluzan pool drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.

Kia is recalling 2022–2026 Carnival vehicles for fuel leak risk at the fuel pipe connection.

Genesis is recalling GV70, G90, G80, and GV80 models over fuel leak risk at pipe connection.

Bentley is recalling 2026 Bentayga vehicles with incorrect tire placard weight capacity labels.

Nissan is recalling 2009-2010 Cube vehicles because the driver’s air bag inflator may detach during deployment, increasing injury risk.

HydroPeptide Clear Alliance Serum recalled due to benzene contamination.
4 products
Cipla recalls Cinacalcet HCl 30 mg tablets over N-Nitroso impurity above acceptable limit.
3 products
Exchange Select Honey Lemon Cough Drops recalled over quality concerns from FDA inspection.
15 products
Remel is recalling Yeastone Broth due to the potential for incorrect antimicrobial susceptibility testing results.

LinkBio CORE Workstation (87-9136) may display incorrect Planning Date on Start Case menu.
Philips is recalling AneurysmFlow software because the MAFA ratio provides unreliable prognostic data for aneurysm treatment decisions.

Arjo Tenor patient lifts (Models KHA1000 US, KHA1010 US) recalled for actuator failure risk causing sudden arm drop.

BISSELL is recalling Steam Shot handheld steam cleaners due to a burn hazard from attachments that can detach and expel hot water or steam.

Easymake adult portable bed rails are recalled due to an entrapment and asphyxiation hazard that violates federal safety standards.

SCUBAPRO is recalling Monorail Weight Pockets for BCDs because the D-ring handle can detach, posing a drowning hazard.

Maitys magnetic drinkware charms are recalled due to an ingestion hazard from loose magnets that can cause serious injury or death.

The products lack required child-resistant packaging, posing a risk of serious injury or death from poisoning if swallowed by young children.

Wybotics is recalling Osprey 700 Max and S1 robotic pool vacuums due to battery overheating, posing burn and fire hazards.

Silks children's loungewear sets are recalled for violating federal flammability standards, posing a serious burn risk to children.

SNOOZ is recalling Breez 2-in-1 Smart Bedroom fans due to an overheating fire hazard caused by power connector corrosion.

Cipla recalls Lanreotide Injection 120 mg/0.5 mL over sterility assurance concerns.
2 products
GE Healthcare recalls Omnipaque (iohexol) Injection 350 mg/mL due to particulate matter.
2 products
Honda is recalling 2018–2022 Odyssey vehicles; side air bags may deploy unexpectedly due to software error.

Chrysler is recalling 2026 Jeep Cherokee vehicles for brake module failure that disables ABS and electronic stability control.
2 products
Thomas Built Saf-T-Liner C2 school buses (2024–2027) may lose warning lights and stop sign due to door switch software defect.

International is recalling 2022–2027 IC Bus EVSB school buses; high voltage disconnect switch may fail to cut power.

Chrysler is recalling 2026 Jeep Wrangler vehicles over insufficient child seat tether welds that may reduce crash restraint.

Nova Bus is recalling Ricon hidden frame windows due to inadequate adhesion that may cause glass detachment during a crash.

Chrysler is recalling 2025–2026 Ram 1500/2500/3500/4500/5500 vehicles over instrument panel display failure that hides critical safety information.

Akron 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.

Stryker is recalling tourniquet cuffs that may detach from the bladder, preventing the device from maintaining pressure.

Imu-Tek recalls Colostrum-5 capsules and powder due to under-processing.
2 products
Divided Sunset Multi Collagen Peptides are recalled for failing to declare egg and fish allergens on the product label.

Viatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.

Toyota is recalling 2015–2022 Lexus RC, 2016–2020 GS, and 2022 IS vehicles over fuel pump failure risk.

Forest River is recalling 2026 Westbrook and Avenger travel trailers with incorrect dry weight labels that may cause overloading and crash risk.

Fagron recalls Vancomycin HCl 1.5g/250mL injection due to sterility concern.
5 products
Geri-Care Artificial Tears Lubricant Eye Drops (0.5 oz, NDC 68788-7266-0) recalled due to lack of sterility assurance.

Siemens is recalling ARTIS pheno and ARTIS Icono X-ray systems (Models 10849000, 11327600, 11328100, 11327700) due to erroneous dose display during patient exams.
