FDA•CRITICAL
Blue Bull Extreme Male Enhancement Supplement
Blue Bull Extreme male enhancement supplement is recalled for containing undeclared sildenafil, which poses serious health risks.
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FDA•MODERATELanreotide Injection 120 mg/0.5 mLCipla is recalling Lanreotide Injection 120 mg/0.5 mL due to a lack of assurance of sterility.
2 products
NHTSA•MODERATEMicro Bird G5 Transit Bus Wheelchair Tie-DownMicro Bird is recalling 2026 G5 transit buses with wheelchair tie-downs that may not lock due to installation error.
NHTSA•MODERATEAltec Service Body and Aerial Device VehiclesAltec is recalling 2023–2026 Service Body and Aerial Device vehicles with incorrect tire pressure labels that may cause blowout or crash.
NHTSA•MODERATEMicro Bird Transit Bus Wheelchair Tie-DownMicro Bird is recalling MB II, G5, and T-Series transit buses with wheelchair tie-downs that may not lock due to installation error.
NHTSA•MODERATENew Flyer Transit Bus Accelera ELFA 3 Control SystemNew Flyer is recalling XE35, XE40, XE60, XHE40, and XHE60 transit buses with Accelera ELFA 3 control systems over unintended acceleration/deceleration risk.
NHTSA•MODERATEMicro Bird School Bus Wheelchair Tie-DownMicro 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.
NHTSA•MODERATECummins PD7000 Electric Drive System Control ModuleCummins PD7000 Electric Drive (part BES CM0904 EV104B) recalled for SCM software error causing unintended vehicle movement.
NHTSA•MODERATENissan Kicks and Sentra Front Seat FrameNissan is recalling 2026 Kicks and Sentra vehicles with insufficiently welded front seat frames that may loosen during a crash.
FDA•MODERATENoromycin 300 LA Oxytetracycline InjectionMWI Animal Health is recalling Noromycin 300 LA oxytetracycline injection (NADA# 141-143) due to lack of assurance of sterility.
FDA•MODERATEMagellan LeadCare II Blood Lead Test KitsMagellan is recalling LeadCare II Blood Lead Test Kits due to a risk of false positive results when used with certain collection devices.
4 products
FDA•CRITICALHalyard Cardiac Cath Pack Syringe AdaptorAVID Medical is recalling cardiac catheterization kits due to a risk of syringe adaptor disconnection during use.
10 products
FDA•MODERATEBuprenorphine Hydrochloride Injection 0.3mg/mLEndo USA recalls Buprenorphine Hydrochloride Injection 0.3mg/mL vials (NDC 42023-179-05) due to particulate matter contamination.
FDA•Favorina Chocolate LadybugsFavorina Chocolate Ladybugs are being recalled due to undeclared hazelnuts, which pose a risk to consumers with nut allergies.
CPSC•17 Stories Furniture 14-Drawer Dressers17 Stories 14-Drawer Dressers recalled for tip-over and entrapment hazards; wall anchoring required. Models 55SCDR14KD* sold via Wayfair Sept 2023–Jan 2026.
CPSC•ProRider Bicycle HelmetsProRider is recalling five bicycle helmet models (BG-W/10, BG-14, SPORT BMX, BM-5 Toddler) due to failure to meet safety standards for impact protection and stability.
CPSC•LIVEHOM 11-Drawer DresserLIVEHOM 11-Drawer Dressers sold on Amazon (Dec 2025–Jan 2026) pose tip-over and entrapment hazards to children without wall anchoring.
CPSC•Kluster Magnet Chess GamesStoney Games is recalling Kluster Magnet Chess Games with loose high-powered magnets posing serious ingestion hazard to children.
CPSC•Playground Swing Set Seats (Model 999604)LFTE USA recalls Playground Swing Set Seats (Model 999604) due to rivet failure posing a fall hazard to children.
FDA•MODERATETreasured Harvest Chilli Spanish PeanutsTreasured Harvest Chilli Spanish Peanuts are being recalled due to potential glass contamination.
2 products- FDA•MODERATEFavorina Chocolate Ladybugs German-Style Nougat
Lidl is recalling Favorina Chocolate Ladybugs (3.52 oz) due to undeclared tree nut allergen on label.
NHTSA•MODERATEHonda CMX300, CMX500, CL500 Handlebar Lock ScrewHonda is recalling 2023–2025 CMX300, CMX500, and CL500 motorcycles; handlebar lock screw may detach and interfere with steering.
NHTSA•MODERATERolls-Royce Cullinan Seat Belt WebbingRolls-Royce is recalling 2020–2026 Cullinan vehicles; loose bolts may damage rear seat belt webbing and reduce crash protection.
NHTSA•CRITICALVision Wheel Aftermarket Aluminum WheelsVision 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.
NHTSA•MODERATEGillig Low Floor Transit Bus Air Compressor Intake PipeGillig is recalling 2021–2026 Low Floor transit buses over air compressor intake pipe contacting fuel line, risking fuel leak and fire.
NHTSA•MODERATEJeep Wagoneer S Liftgate Hinge CoverChrysler is recalling 2024–2026 Jeep Wagoneer S vehicles; liftgate hinge cover may detach and create a road hazard.
NHTSA•MODERATEGillig Low Floor Transit Bus High Voltage CableGillig is recalling 2023–2026 Low Floor transit buses over high voltage cable overheat and fire risk.
FDA•MODERATEB.R.A.H.M.S PlGF Plus KRYPTOR In Vitro Diagnostic TestB.R.A.H.M.S PlGF Plus KRYPTOR (Catalog 859075N) recalled for out-of-range quality control values that may cause falsely elevated preeclampsia risk results.
FDA•MODERATEStryker Sustainability Solution Tourniquet CuffsStryker is recalling tourniquet cuffs that may fail to maintain pressure due to a potential welding connection detachment.
FDA•MODERATEARTIS Pheno VE30A and VE40A Imaging SystemSiemens is recalling ARTIS Pheno VE30A and VE40A imaging systems (Model 10849000) due to unregulated dose causing unintentional low-dose radiation exposure.
FDA•MODERATEMesh Style Tip ProtectorsHealthmark Industries is recalling Mesh Style Tip Protectors (models CSW-03-2.0 and CSW-04-4.0) due to a lack of FDA clearance.
FDA•CRITICALDouble Down Deer Feed ProductsProducers Cooperative Association recalls Double Down Deer Feed products (SKUs 12254, 12750, 13380, 13381) over aflatoxin contamination exceeding safe limits.
2 products
FDA•MODERATELinkBio CORE WorkstationLinkBio CORE Workstation (87-9136) may display incorrect Planning Date on Start Case menu.
FDA•CRITICALOmnipod 5 PodsInsulet is recalling Omnipod 5 Pods due to a cannula tear that can cause insulin leakage, leading to dangerous under-delivery of insulin.
FDA•MODERATEiLet Bionic PancreasBeta Bionics is recalling iLet Bionic Pancreas (software 1.4.2–1.4.3) for Dexcom G7 compatibility issues that may disable glucose correction dosing.
FDA•LOWYunker Energy & Health Herbal SupplementSato Pharmaceutical is recalling Yunker Energy & Health Herbal Supplement because it does not meet label claims for Vitamin E content.
FDA•CRITICALSpray Dried Dairy PowderLone Star Dairy Products is recalling Spray Dried Dairy Powder (25 kg bags, 1 metric ton totes) due to Salmonella contamination.
FDA•MODERATETETAS Mireya Cherry Milkshake PopsicleASUKAR FOODS CORP is recalling TETAS Mireya Cherry Milkshake popsicles (UPC 83822654822) due to undeclared soy lecithin.
FDA•MODERATE0.9% Sodium Chloride Injection, USPFresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP, 250 mL bags due to a lack of assurance of sterility.
14 products
NHTSA•MODERATEATC PL700 and PL750 Recreational TrailersATC is recalling 2023–2026 PL700 and PL750 trailers over carbon monoxide entering the cabin from generator exhaust.
NHTSA•MODERATEMack TerraPro Engine Control Unit SoftwareMack is recalling 2022–2027 TerraPro trucks; ECU software may allow engine start in gear, risking unexpected movement.
NHTSA•MODERATEVolkswagen Jetta Transmission Ground WireVolkswagen is recalling 2025–2026 Jetta vehicles over loose transmission ground wire fire risk.
NHTSA•MODERATEVolvo EX30 Seat Belt Warning SystemVolvo is recalling 2025–2026 EX30 and 2026 EX30CC vehicles over a faulty seat belt warning chime system.
NHTSA•MODERATEARBOC Spirit of Freedom/Mobility Rear ABS SystemARBOC is recalling 2018–2026 Spirit of Freedom/Mobility buses over rear ABS malfunction that increases crash risk.
FDA•MODERATEB Braun IV Administration SetsWindstone Medical is correcting B Braun IV administration sets due to potential medication backflow and priming occlusion risks.
3 products
FDA•MODERATEMedtronic Sphere-9 Cardiac Ablation CatheterMedtronic Sphere-9 Catheter (Model AFR-00001) may cause ventricular fibrillation in patients with Biotronik ICDs or CRT-Ds during radiofrequency ablation therapy.
FDA•MODERATEArrow Echogenic Introducer NeedleArrow International is recalling the Echogenic Introducer Needle due to a supplier notice regarding incorrectly manufactured liquid adhesive.
13 products
FDA•CRITICALIntuitive SureForm 30 Gray ReloadsIntuitive Surgical is recalling SureForm 30 Gray Reloads (Ref 48230M-05, 48230M-06) due to the risk of an incomplete staple line.
FDA•CRITICALCostco Service Deli Meatloaf SeasoningGriffith Foods is recalling Costco Service Deli Meatloaf Seasoning due to potential Salmonella contamination.
3 products
FDA•MODERATEHorizon Organic Chocolate Lowfat MilkHorizon Organic is recalling chocolate lowfat milk in 8-oz cartons due to compromised package integrity.