All Recalls

Cardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.

BMW is recalling 2017–2025 K 1600 GT/GTL/B and 2018–2025 Grand America motorcycles over reverse gear control unit overheating and fire risk.

GM recalls 2023–2025 Chevrolet Malibu rearview cameras that may display distorted or blank images.

GM is recalling 2025–2026 Chevrolet Corvette models over a software error that may prevent detection of rear turn signal failure.

Keystone is recalling 2026 Montana fifth wheel trailers; underbelly may detach during transit, creating road hazard.

Mei Heong Yuen roasted peanuts recalled over banned cyclamate sweetener.

American Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.

Civco recalls eTRAX Needle System Starter Kit 12G (Part 667-149) due to sensor programming error causing incorrect needle tip position.

Volvo is recalling 2025–2027 VNL and 2026–2027 VNR trucks over turn signal failure risk.

Audi is recalling 2026 Q3 vehicles for sunroof software that allows remote closing without operator visibility.

Isuzu is recalling 2025–2027 Chevrolet Low Cab Forward and Isuzu NRR vehicles over improperly secured wire harnesses that may chafe, causing engine stall, brake failure, or fire.

Mack is recalling 2025–2027 Pioneer and 2027 Anthem trailers with non-functional turn signals that increase crash risk.

Appco Pharma recalls Prazosin HCl 1mg capsules over nitrosamine impurity (NNP) above acceptable limits.

K.C. Pharmaceuticals recalls multiple brands of sterile eye drops over sterility concerns.

Ricon is recalling R1200 series Power Transfer Seat Base units over potential gear motor locking failure.

Ford is recalling 2026 Explorer and Mustang vehicles for incorrectly installed piston circlips that may cause engine failure and loss of drive power.

Nova Bus is recalling 2025 and 2024 LFS Artic transit buses; window glass may detach due to inadequate frame adhesion.

Toyota is recalling 2023–2025 Corolla Cross Hybrid vehicles for insufficient pedestrian warning sounds in reverse.

Ford is recalling 2025–2026 Bronco Sport and Maverick vehicles; front passenger air bag may not deploy due to OCS sensor failure.

Ford is recalling 2021–2023 Lincoln Navigator, Expedition, and 2022–2023 F-Series Super Duty trucks due to windshield wiper arm breakage.

Ford is recalling 2026 Lincoln Aviator and Explorer vehicles for HVAC system failure affecting windshield defrosting.

JFE recalls Dumpling Party Trays and Loaded Dumpling Vegetable products over possible glass contamination.

Amneal is recalling 500-count bottles of Tramadol Hydrochloride 50 mg tablets due to an impurity found during stability testing.

Chiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.

Synthes recalls VOLT Locking and Cortical Screw Taps due to incorrect thread from a lot swap.

Olympus recalls SOLTIVE laser systems (TFL-SLS, TFL-PLS) due to power supply defect that may cause inoperability and smoke.

Aston Martin is recalling 2021–2026 DBX models due to rear suspension arm pin failure risking loss of control.

Terex is recalling pole guide arm assembly pins (part 450543) due to cracked welds that may cause the arm to fall.

Vital Nutrients Aller-C is recalled due to undeclared egg, soy, and hazelnut allergens.

4our Kiddies furniture tip restraint kits are recalled because the plastic components can break, posing tip-over and entrapment hazards.

AirClub convertible bassinets are recalled due to a fall hazard caused by a defective attachment mechanism that violates federal safety standards.

MPINOI adult portable bed rails are recalled due to a serious entrapment and asphyxiation hazard that violates federal safety standards.

GLMZZ Fidget Magnet Ball Toys are recalled due to a serious ingestion hazard that violates federal toy safety standards.

FUNTOK 24V 2-seater ride-on trucks (model DLS-K03) are recalled due to fire and burn hazards from an overheating circuit board.

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

CCCEI power strips are recalled due to a fire hazard caused by a lack of overcurrent protection.

Petzl is recalling Nomic and Ergonomic ice climbing axes due to a shaft breakage hazard that poses a risk of serious injury or death.

DIY Sauna Heater Kits are being recalled due to an overheating issue that poses a fire hazard and risk of serious injury or death.

Vive Health is recalling adult portable bed rails due to entrapment and asphyxiation hazards that have resulted in two deaths.

Teva recalls Octreotide Acetate 20 mg vials over sterility assurance concerns.

A recall was issued for Artoura Breast Tissue Expanders due to infusion sets that may contain dull or blunt needle tips.

Philips recalls Allura Xper FD10/FD20 systems over wired foot switch failure causing intermittent X-ray imaging.

Medline recalls ENFit G-tube connectors in care/discharge kits over seal failure and leakage risk.

Waldemar Link recalls Embrace Drill Tower instruments over mixed-up article numbers in the surgical technique overview.

Ultradent is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011, due to crumbling and breakage risk.

RefleXion X1 Radiotherapy System Model RXM1000 recalled for software defect causing incorrect radiation dose delivery.

Medline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.

Stryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System due to a potential ceiling cover support failure.

ReCor Medical is recalling the Paradise Ultrasound Renal Denervation Catheter (Model PRDS-068-02) as these units were intended to be scrapped.

Philips Vue Motion V12 (1017979) may display image frames out of sequence during dynamic imaging runs.