All Recalls

Grand Design is recalling 2026-2027 Lineage RVs with MaxxAir N-Series rooftop fans due to an overheating circuit board that poses a fire risk.

Zoox is recalling ADS software that may fail to detect heavy smoke, increasing the risk of a crash in low-visibility conditions.

Insignia gas ranges (models NS-RGFGSS1 and NS-RGFCGS2) are recalled due to a fire hazard from knobs that can be accidentally activated.

Flaunt is recalling MagSafe Battery Charger model E33A due to fire and burn hazards from the lithium-ion battery overheating.

Greenworks is recalling 20+ models of Kobalt yard power tools due to a fire hazard when charging batteries via the USB-C port.

Moodooy model F311 adult portable bed rails are recalled due to serious entrapment and asphyxiation hazards.

WonderStone infant walkers are recalled due to a fall hazard; they fail to meet mandatory safety standards for doorway and step-edge stopping.

CMR Surgical is recalling the Versius Surgeon Console due to a cybersecurity risk involving the Secure Boot feature.

Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays because a loose knob may cause surgical misalignment.

Integra LifeSciences is recalling the OmniTract Surgical Retractor System due to insufficient drying time instructions in the user manual.

The GSP Neonatal GALT Kit is recalled due to reduced on-board stability, which may cause test failures and delays in patient results.

Elekta recalls Fletcher CT/MR applicator set due to risk of IU tube tip detachment.

Volvo is recalling 2026 VHD, VNL, VNR, VN, and VAH trucks due to a risk of steering control loss from loose steering arm fasteners.

Somerset Therapeutics recalls Pemetrexed for Injection 100mg/Vial due to cGMP deviations.

Klowen is recalling the Custom Orthodontic Solution, model CIAS-800033, due to a defect that may cause incorrect bracket placement.

Siemens is recalling the Atellica CH Enzymatic Hemoglobin A1c assay (Material No. 11097536) due to potential for inaccurate patient results.

Medline recalls Anesthesia Kit Peds 90-LF due to included temperature probe distribution error.

Gasco recalls Isopropyl Alcohol 70% in multiple sizes due to subpotency, which may reduce antiseptic effectiveness.

Fresenius recalls 5008X Blood Tubing Sets over potential online port errors.

Boston Scientific is recalling Intracept Access Instruments due to a potential sterile barrier breach that could lead to severe infection.

Masimo recalls Radius VSM NIBP cuffs and ECG sets over false heart-rate alarms and cuff edge irritation.

BMW is recalling certain 530e, 740Le, and 330e iPerformance vehicles due to an engine starter relay that may corrode and cause a fire.

KTM is recalling certain Husqvarna and GasGas motorcycles because the rear brake caliper may crack and break, reducing braking ability.

PACCAR is recalling certain 2026-2027 Peterbilt 579 and 2027 Kenworth T680 tractors due to an incorrectly installed air brake valve.

Forest River is recalling 2026-2027 Wildwood and Salem travel trailers due to an incorrect GVWR on the Federal Placard.

Toyota is recalling 2026 Lexus TX and Toyota Grand Highlander vehicles due to a risk of rear axle carrier breakage and loss of vehicle control.

Shyft is recalling 2016, 2019, and 2021 Utilimaster Velocity vehicles due to a strobe light short circuit that poses a fire risk.

BMW recalls certain 2023-2026 models over starter motor fire risk.

QuVa Pharma is recalling Methohexital Sodium 100 mg/10 mL vials due to failed impurities and degradation specifications.

Medline Remedy Specialized Silicone Cream is recalled due to an out-of-specification result for formaldehyde in the raw material.

Avet Pharmaceuticals is recalling Methohexital Sodium for Injection 500 mg vials due to failed impurities and degradation specifications.

ConvaTec is recalling Aquacel Ag Surgical SP dressings because they were manufactured with a thickness exceeding specifications.

Olympus is replacing the previous design of the MAJ-2315 Single Use Distal Cover used with the EVIS EXERA III Duodenovideoscope.

Braun is recalling 2026 Chevrolet Traverse vehicles due to a missing braze connection in the fuel fill line that poses a fire risk.

Harbor Freight is recalling Kenway towing and submersible lights that may fail to illuminate, increasing the risk of a crash.

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

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.

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.

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.

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.

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.