
NHTSA•MODERATE
Audi 2026 Q3 Sunroof System
Audi is recalling 2026 Q3 vehicles for sunroof software that allows remote closing without operator visibility.

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.
3 products
K.C. Pharmaceuticals recalls multiple brands of sterile eye drops over sterility concerns.
15 products
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.
7 products
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.
2 products
Olympus recalls SOLTIVE laser systems (TFL-SLS, TFL-PLS) due to power supply defect that may cause inoperability and smoke.
2 products
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.
6 products
A recall was issued for Artoura Breast Tissue Expanders due to infusion sets that may contain dull or blunt needle tips.
7 products
Philips recalls Allura Xper FD10/FD20 systems over wired foot switch failure causing intermittent X-ray imaging.
22 products
Medline recalls ENFit G-tube connectors in care/discharge kits over seal failure and leakage risk.
2 products
Waldemar Link recalls Embrace Drill Tower instruments over mixed-up article numbers in the surgical technique overview.
2 products
Ultradent is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011, due to crumbling and breakage risk.

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

Medline is recalling Puracol and Puracol Plus wound dressings due to elevated endotoxin levels that may cause severe inflammatory responses.

Yamaha is recalling 2026 TW200 motorcycles with speedometer failure that may increase crash risk.

Luxfer is recalling gas cylinder adapters (model EP-O-350-8-U5) due to O-ring incompatibility risking hydrogen leak and fire.
2 products
Mercedes-Benz is recalling 2025 G580 vehicles with incorrect wheel bolts that may loosen or detach.

Mercedes-Benz is recalling 2026 GLE and GLS models over passenger air bag fabric defect that may prevent deployment.

KTM is recalling 2022–2024 390 Duke and RC 390 motorcycles due to throttle control unit water ingress causing loss of power.

Triumph is recalling 2026 Trident 800 motorcycles with improper headlight low beam illumination that increases crash risk.

Siemens is recalling the Atellica CH A1c_E assay due to a risk of depressed results when used alongside the RCRP assay on the same analyzer.

American Laboratories recalls pepsin powders (Full Strength, 1:10,000, 1:3000) due to potential Salmonella contamination.
3 productsPhilips Respironics recalls Trilogy Evo ventilators over tidal volume discrepancy with non-pneumatic nebulizers.
4 products