NHTSA•MODERATE
Tiffin Motorhomes GT1, GH1, GH2 Seating Capacity Label
Tiffin is recalling 2025–2026 GT1, GH1, and 2026 GH2 motorhomes with incorrect seating capacity labels that may result in unbelted passengers.
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NHTSA•MODERATEFord F-59 and F-53 Brake LightsFord is recalling 2025–2026 F-59 and F-53 chassis vehicles; brake lights may remain illuminated when not braking, increasing crash risk.
NHTSA•MODERATEForest River Entourage Motorhome CCC LabelForest River is recalling 2025–2026 Entourage motorhomes with incorrect CCC labels stating 7 belted seats instead of 8, risking overload and crashes.
FDA•MODERATEAlbuterol Sulfate Inhalation Solution 0.5%Nephron SC recalling Albuterol Sulfate Inhalation Solution (NDC 69374-330-05) due to illegible labeling.
FDA•MODERATELucerne 2% Cottage CheeseAlbertsons is recalling Lucerne 2% Cottage Cheese due to potential contamination with metal fragments.
FDA•LOWPopping Boba RTD Mixed Berry Hibiscus TeaPocas International is recalling Popping Boba RTD Mixed Berry Hibiscus Tea due to a packaging integrity issue.
4 products
FDA•MODERATEMeclizine Hydrochloride Tablets 12.5 mgAmerican Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.
NHTSA•MODERATEOrange EV Terminal Truck Training SeatOrange 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.
NHTSA•MODERATEFerrari 12Cilindri WindowsFerrari is recalling 2025–2026 12Cilindri vehicles with dark-tinted windows that reduce driver visibility and fail safety standards.
FDA•MODERATECinacalcet Hydrochloride TabletsCipla is recalling Cinacalcet Hydrochloride Tablets due to the presence of N-Nitroso Cinacalcet above acceptable limits.
3 products
FDA•MODERATEMedline CENTURION Circumcision KitMedline is recalling CENTURION Circumcision Kit (CIT7050F) due to one lot distributed without sterilization.
FDA•MODERATEAccess Total T4 CalibratorBeckman Coulter is recalling Access Total T4 Calibrator (Catalog No. 33805) due to negative bias causing falsely low results on DxI 600/800 instruments.
FDA•MODERATEFlamingo Funnel SmallSurgiSmoke Solutions is recalling the Flamingo Funnel Small due to a manufacturing error involving non-gamma compatible sterilization drapes.
3 products
FDA•MODERATEMedline Universal Central/Art Line Insertion KitMedline is recalling convenience kits containing non-sterile alcohol prep pads due to potential bacterial contamination.
10 products
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 Diagnostics LeadCare II Blood Lead Test KitsMagellan Diagnostics is recalling LeadCare II blood lead test kits due to the risk of false positive results.
4 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•MODERATETreasured Harvest Chilli Spanish PeanutsTreasured Harvest Chilli Spanish Peanuts are recalled due to potential glass contamination.
2 products
FDA•MODERATEFavorina Chocolate Ladybugs German-Style NougatLidl 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•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 detachment at the welding connection.
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•MODERATELinkBio CORE WorkstationLinkBio CORE Workstation (87-9136) may display incorrect Planning Date on Start Case menu.
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•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 Infusion Pump Administration SetsWindstone Medical Packaging is recalling Pre Op Kits containing B Braun IV administration sets due to potential medication backflow or priming issues.
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 is recalling the Echogenic Introducer Needle due to a manufacturing error involving the device's liquid adhesive.
13 products
FDA•MODERATEHorizon Organic Chocolate Lowfat MilkHorizon Organic is recalling chocolate lowfat milk in 8-oz cartons due to compromised package integrity.