All Recalls

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

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.

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.

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.

Zimmer Surgical recalls A.T.S. 4000 TS Tourniquet Dual Hose (Model 60-1812-101-00) due to sterility breach risk.

W.L. Gore & Associates is recalling its GORE TAG Thoracic Branch Endoprosthesis due to a device defect.

Bard recalls acute drainage trays due to lidocaine ampoules made under deficient practices.

Medline is recalling gravity sets labeled "Not for Human Use" that were inadvertently shipped to the U.S. market.

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.

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.

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.

Warn is recalling wireless remote kits (part numbers 90287 and 90289) that may cause unexpected winch movement, posing an injury risk.

Eunha Fisheries recalls Korean halibut and flounder sashimi due to undeclared wheat, soy, sesame, Yellow #5, and Blue #1.

Lupin recalls Glucagon Emergency Kits due to a stability test failure that may impair emergency use.

PH Labs recalls Ocular Plus and Vista MAX supplements due to undeclared Yellow #5.

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.

RaySearch recalls RayCare 2024A SP1 oncology software due to potential data loss in beam set delivery notes.

Medela is recalling ENFit Enteral Extension Sets due to incorrect connectors that may cause delivery delays or misconnections.

Accuray is recalling the Xchange Robotic Collimator Changer for the Cyberknife system due to a risk of the collimator falling from its housing.

Siemens recalls ARTIS icono biplane over potential loss of movement after detector lift height adjustment.

Accuray is recalling the Cyberknife Xchange Robotic Collimator Changer due to a risk of the component falling from its housing.

Boston Scientific recalls CRE Pro Wireguided dilator due to potential sterile pouch breach.

The IntelliCuff pressure controller may fail to maintain cuff pressure due to a system leakage error, causing the motor to run continuously.

Teleflex is recalling Pilling Wecksorb Neurosponges and Neurosponge Strips due to potential out-of-specification levels of endotoxins.

Baxter is recalling the Adapter for Head Positioning due to a risk of the accessory becoming loose and moving during patient positioning.

Honda is recalling 2018-2020 Odyssey vehicles because water intrusion can cause the rearview camera to fail, increasing the risk of a crash.

BMW is recalling various 2023-2025 BMW, Mini, and Rolls-Royce vehicles due to an integrated brake system malfunction that increases crash risk.

Chrysler is recalling Mopar headlights that may flicker or fail, reducing vehicle visibility and violating federal safety standards.

Chrysler is recalling 2026 Ram 1500 vehicles due to headlight wiring issues that may cause parking and daytime running lights to fail.

Honda is recalling 2026 Pilot and Passport vehicles due to improperly tightened rear subframe bolts that may cause stability loss.

Boehringer Ingelheim is recalling Synjardy XR tablets due to manufacturing deviations involving improper cleaning and sampling of production equipment.