
NHTSA•MODERATE
Subaru Crosstrek, Forester, and Ascent Certification Labels
Subaru is recalling various Crosstrek, Forester, and Ascent models due to incorrect weight rating labels that may lead to vehicle overloading.

Subaru is recalling various Crosstrek, Forester, and Ascent models due to incorrect weight rating labels that may lead to vehicle overloading.

Ola-Ola Pounded Yam recalled for undeclared milk allergen; EXP Nov 2028–May 2029.

Wabash is recalling 2021-2026 Econex Refrigerated Body vehicles because the side door stirrup steps may detach, posing injury and crash risks.

Tesla recalls certain 2026 Model Y and 2024 Model 3 vehicles lacking knee air bags and other safety features.

Ola-Ola Pounded Yam recalled for undeclared milk allergen; EXP Nov 2028–May 2029.

Adams Extract recalls multiple seasonings due to undeclared sesame allergen.
5 products
Prime-Time is recalling Q'Straint Max wheelchair retractors in 2025-2026 Ford Med Transit vans that may fail to lock and secure wheelchairs.

Southeast Toyota is recalling one 2026 Tundra truck due to an incorrect load carrying capacity label that violates federal safety standards.

Frutas y Hortalizas del Sur S.A. is recalling 10 oz bags of Organic Whole Blueberries due to potential E. coli O145:H28 contamination.

Mars Petcare is recalling Pedigree High Protein Chopped Ground Dinner over potential contamination with plastic and metal foreign material.

FSIS issued a public health alert for a ready-to-eat beef jerky product due to misbranding and an undeclared wheat allergen.

Fusia Kimchi & Tofu Kimbap recalled due to undeclared fish allergen.

AMASKY nursing pillows are recalled due to a suffocation hazard, as they violate federal safety standards for infant support cushions.

Conair is recalling 10+ models of Cuisinart grill brushes because detached metal bristles pose an ingestion and internal injury hazard.

Cooper Lighting is recalling Metalux Optimized High Bay LED light fixtures due to a fire hazard from potential overheating.

CVS Health Medicated Hemorrhoidal Wipes are recalled due to non-child-resistant packaging, posing a risk of poisoning to young children.

Junpower CR2032 lithium coin batteries are recalled for lacking child-resistant packaging, posing a severe ingestion and chemical burn hazard.

POPOOO LED finger lights are recalled due to a risk of serious injury or death from button cell battery ingestion.

Rowenta is recalling cordless vacuum batteries that can overheat and ignite, posing fire and burn hazards.

Gigglescape Under the Sea Popping Toys are recalled due to a choking hazard caused by a detachable plastic dome.

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

Vevor is recalling baby loungers due to fall and entrapment hazards that violate federal safety standards for infant sleep products.

Winco Fireworks is recalling Roman Candles 8 Shot fireworks (Model RCLR-W8012) due to explosion and burn hazards from tube malfunctions.

Winco Fireworks is recalling Unity 7 Shot aerial fireworks (model MEF6096) due to tip-over, explosion, and burn hazards.

Cipla recalls Cinacalcet HCl 30 mg tablets due to nitrosamine impurity above ADI.
3 products
Lannett is recalling 5 mg Dextroamphetamine/Amphetamine ER capsules due to a labeling mix-up where capsules contain immediate-release pellets.

Asclemed recalls Accucaine kits and Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL ampules due to lack of sterility assurance.
2 products
Zimmer Surgical recalls A.T.S. 4000 TS Tourniquet Dual Hose (Model 60-1812-101-00) due to sterility breach risk.
2 products
W.L. Gore & Associates is recalling its GORE TAG Thoracic Branch Endoprosthesis due to a device defect.
2 products
Medline is recalling reprocessed catheters due to residual particulate matter that may cause infection or embolism.

Bard recalls acute drainage trays due to lidocaine ampoules made under deficient practices.
20 products
Medline is recalling gravity sets labeled "Not for Human Use" that were inadvertently shipped to the U.S. market.

Medtronic is recalling the Harmony Delivery Catheter System due to a manufacturing defect that may cause the distal tip to detach during use.

Laborie is recalling Solar GI System configurations due to moisture accumulation that may affect pressure measurement performance.

Covidien recalls Shiley Disposable Decannulation Plug over incorrect non-DEHP labeling; product contains 30-35% DEHP.
2 products
Jayco is recalling 2026 Heartland Cyclone trailers due to a missing inverter ground connection that poses fire and electrical shock risks.

Jayco is recalling 2026 Seismic fifth toy haulers due to a missing grounding connection that poses fire and electrical shock risks.

Kia is recalling 2020-2024 Telluride vehicles due to a risk of fire from overheating front power seat motors.

Hyundai is recalling 2023-2024 Ioniq 5 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.

Kia is recalling 2022-2024 EV6 and 2024 EV9 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.

Altec is recalling 2022-2026 Service Body vehicles due to a wiring defect that may cause a short circuit and increase the risk of fire.

Nissan is recalling 2026 Leaf vehicles because rear seat belt retractors may fail to properly secure child restraint systems.

Crestline is recalling 2026 Ford CCL166 Type III emergency vehicles due to a fuel line puncture risk that may cause a fire.

Warn is recalling wireless remote kits (part numbers 90287 and 90289) that may cause unexpected winch movement, posing an injury risk.
2 products
Eunha Fisheries recalls Korean halibut and flounder sashimi due to undeclared wheat, soy, sesame, Yellow #5, and Blue #1.
2 products
Lupin recalls Glucagon Emergency Kits due to a stability test failure that may impair emergency use.
3 products
PH Labs recalls Ocular Plus and Vista MAX supplements due to undeclared Yellow #5.
2 products
Hikma is recalling Gemcitabine Injection due to improper temperature storage.

Zeiss is recalling the 1.5 cm Intrabeam Spherical Applicator (REF 304534-6000-557) due to failure to meet manufacturing specifications.

Siemens is recalling the ARTIS icono ceiling suspension (Model 11328100) because monitor attachment screws may loosen over time.
