All Recalls

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 over N-nitroso impurity above safe limit.

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 ampules over sterility concerns.

Zimmer Surgical recalls A.T.S. 4000 TS Tourniquet Dual Hoses over sterility breach risk.

Gore is recalling 30+ models of the TAG Thoracic Branch Endoprosthesis Side Branch Component due to a risk of catheter separation.

Bard recalls Acute Drainage trays due to deficient lidocaine ampoules from supplier.

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

Covidien is recalling 12+ models of Shiley Disposable Decannulation Plugs due to incorrect labeling regarding DEHP content.

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.

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

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 over beam set delivery note data loss risk.

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 detector lift movement.

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 Dilatation Balloons over 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.

Accord Healthcare is recalling 300 mcg Levothyroxine Sodium Tablets due to subpotency.

Lupin Pharmaceuticals is recalling three sizes of prednisoLONE Acetate Ophthalmic Suspension 1% due to the presence of a foreign substance.

Remel is recalling GC Agar Base plates due to a risk of reduced or no recovery of Neisseria gonorrhoeae strains.

Jayco is recalling 2027 Entegra Accolade and Jayco Seneca motorhomes because missing dinette brackets may cause the seating to detach.

Teko is recalling 2026 Triumph, Turbo, and Trophy vehicles because a missing alert system prevents them from making required pedestrian sounds.

Nissan is recalling JATCO automatic transmission control valve assemblies that may fail to correctly display the selected gear.

Ford is recalling certain 2024-2027 Lincoln Nautilus Hybrid and 2025-2027 Explorer Hybrid vehicles due to a missing pedestrian warning sound.

Ford is recalling 2024–2026 Mustang and 2025–2026 Mustang GTD vehicles because cold weather can cause windshield wiper and washer malfunctions.

Ford is recalling 2021-2023 Mustang Mach-E vehicles due to a risk of rear differential pinion shaft fracture and potential loss of drive power.

Nissan is recalling 2026 Rogue vehicles because the instrument panel may fail to display the gear selection, increasing the risk of a crash.

Chrysler is recalling 2026 Jeep Grand Wagoneer and Grand Wagoneer L vehicles due to a software error that may cause a loss of brake assist.

Chrysler is recalling certain 2022-2024 Jeep Grand Cherokee and Wagoneer vehicles due to a software error affecting the gear selection indicator.

Accord BioPharma is recalling Imuldosa (ustekinumab-srlf) 130 mg/26 mL injection vials due to a lack of assurance of sterility.