Ford is recalling certain 2022–2025 Lincoln Navigator, Nautilus, Aviator, and Explorer vehicles over Image Processing Module resets causing loss of rearview camera and ADAS features.
Diagnostica Stago is recalling the STA Liatest D-Di kit due to a positive bias in D-Dimer measurements that may cause inaccurate test results.
2 products
TETAS Mireya Cherry Milkshake popsicles recalled for undeclared soy lecithin allergen.
Zydus Pharmaceuticals is recalling Icosapent Ethyl Capsules due to oxidation, which can cause capsule melting and discoloration.
Cardinal Health is recalling Webcol Alcohol Prep Pads (200-count boxes) due to microbial contamination that may pose infection risk.
3 products
Welch Allyn is recalling the Spot Vision Screener VS100 (software v3.2.0.1) due to a screen flickering issue that may trigger seizures.
Toyota is recalling Lexus NX350, NX250, RX350, and TX350 vehicles over rearview camera display failure that reduces rear visibility.
Land Rover is recalling 2026 Defender vehicles with defective third-row seat belt anchorage welds that may fail to restrain occupants.
Keystone is recalling 2026 Montana fifth wheel trailers due to improperly secured wiring that may be damaged by the bedroom slide-out, creating fire risk.
2 products
Bluegrass Ingredients recalls Butter-Rich and Butter Powder (50 lb.) over Salmonella risk.
2 products
Ford is recalling 2020–2026 Explorer and Lincoln Aviator vehicles over improperly secured second-row seat belt anchors.
2 products
Hyundai is recalling 2026 Palisade and Palisade Hybrid power rear seats that may fail to detect and trap a person.
Ford is recalling 2025–2026 Maverick vehicles over moonroof glass that may detach and become a road hazard.
Ford is recalling F-Super Duty F250–F550, F600, and F750 vehicles over high pressure fuel pump failure risk due to biodiesel deposits.
Tiffin is recalling 2025–2026 GT1, GH1, and 2026 GH2 motorhomes with incorrect seating capacity labels that may result in unbelted passengers.
Ford is recalling 2025–2026 F-59 and F-53 chassis vehicles; brake lights may remain illuminated when not braking, increasing crash risk.
Forest River is recalling 2025–2026 Entourage motorhomes with incorrect CCC labels stating 7 belted seats instead of 8, risking overload and crashes.
Taro Pharmaceuticals is recalling Children's Ibuprofen Oral Suspension 100 mg/5mL (120 mL) due to gel-like masses and black particles.
GE recalls Centricity Universal Viewer software over credential exposure risk.
4 products
Orange EV is recalling T-Series, e-TRIEVER, and HUSK-e terminal trucks with foldaway training seats that may fail to restrain occupants in a crash.
2 products
Ferrari is recalling 2025–2026 12Cilindri vehicles with dark-tinted windows that reduce driver visibility and fail safety standards.
Playground swing seats (model 999604) are being recalled due to a fall hazard caused by potential rivet failure.
Abbott is recalling ID NOW Influenza A & B 2 test kits (Model 427-000) due to an increased rate of invalid results.
Micro Bird is recalling 2026 G5 transit buses with wheelchair tie-downs that may not lock due to installation error.
Altec is recalling 2023–2026 Service Body and Aerial Device vehicles with incorrect tire pressure labels that may cause blowout or crash.
Micro Bird is recalling MB II, G5, and T-Series transit buses with wheelchair tie-downs that may not lock due to installation error.
New Flyer is recalling XE35, XE40, XE60, XHE40, and XHE60 transit buses with Accelera ELFA 3 control systems over unintended acceleration/deceleration risk.
Micro Bird is recalling MB II, G5, and T-Series school buses (2003–2026) with wheelchair tie-downs that may not lock due to installation error.
Cummins PD7000 Electric Drive (part BES CM0904 EV104B) recalled for SCM software error causing unintended vehicle movement.
Nissan is recalling 2026 Kicks and Sentra vehicles with insufficiently welded front seat frames that may loosen during a crash.
2 products
Insulet is recalling Omnipod 5 Pods due to a cannula defect that can cause insulin under-delivery and severe health risks.
17 Stories 14-Drawer dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.
ProRider is recalling various bicycle helmets that fail federal safety standards, posing a serious risk of head injury or death in a crash.
LIVEHOM 11-Drawer Dressers are recalled due to tip-over and entrapment hazards that pose a risk of serious injury or death to children.
Stoney Games is recalling Kluster magnet chess games due to a serious magnet ingestion hazard that can cause severe internal injury or death.
Medline is recalling cardiac procedure kits to clarify that the included chest drainage units are intended for adult patients only.
Medline is recalling Medcrest surgical gowns due to fabric delamination risks that may lead to infection or delays in patient care.
3 products
Lutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.
Honda is recalling 2023–2025 CMX300, CMX500, and CL500 motorcycles; handlebar lock screw may detach and interfere with steering.
Rolls-Royce is recalling 2020–2026 Cullinan vehicles; loose bolts may damage rear seat belt webbing and reduce crash protection.
Vision Wheel is recalling aftermarket aluminum wheels (part numbers 640-6744GBMF38, 640-6765GBMF40, 640-7710GBMF40, 640-7744GBMF40, 640-7765GBMF40) that may crack and cause loss of vehicle control.
2 products
Gillig is recalling 2021–2026 Low Floor transit buses over air compressor intake pipe contacting fuel line, risking fuel leak and fire.
Chrysler is recalling 2024–2026 Jeep Wagoneer S vehicles; liftgate hinge cover may detach and create a road hazard.
Gillig is recalling 2023–2026 Low Floor transit buses over high voltage cable overheat and fire risk.
Rising Pharmaceuticals is recalling Temozolomide Capsules 5mg (NDC 16571-816-51) due to failed impurities and degradation specifications.
Mylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.
Radnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.
Artelon FlexBand Dynamic Matrix recalled over failed endotoxin testing.
3 products
Beckman Coulter recalls DxC 700 AU and AU5800 analyzers over software delay risk.
2 productsHealthCast is recalling Vital Sync software due to a failure to transmit or receive critical patient bedside monitor alarms.
2 products