NHTSA•MODERATE
2026 Ram 2500 Pickup Electronic Stability Control
Chrysler is recalling 2026 Ram 2500 Pickups with steering column control module defects that disable electronic stability control.
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FDA•MODERATEDesmopressin Nasal Spray, USP 10 mcg/0.1 mLApotex is recalling Desmopressin Nasal Spray (NDC 60505-0815-0) due to defective bottle caps with missing or dislodged liners.
3 products
FDA•MODERATEBooey's Dragon's Breath SauceBooey's Dragon's Breath sauce recalled for undeclared fish and sesame allergens.
FDA•MODERATEMedline CENTURION Circumcision KitMedline is recalling CENTURION Circumcision Kit (CIT7050F) due to one lot distributed without sterilization.
FDA•MODERATEPhilips Spectral CT on RailsPhilips Spectral CT on Rails (Model 728334) requires a software update to address gantry positioning, message display, and menu option issues.
NHTSA•MODERATEWinnebago Suncruiser and Sunflyer Side ReflectorsWinnebago is recalling 2026–2027 Suncruiser and Sunflyer motorhomes with missing side reflectors, increasing crash risk.
NHTSA•MODERATEAudi E-Tron Brake PedalAudi is recalling 2019–2024 E-Tron and 2020–2024 E-Tron Sportback vehicles due to brake pedal detachment risk.
FDA•MODERATEEpinephrine Injection USP 1 mg/10mLInternational Medication Systems is recalling Epinephrine Injection 1 mg/10mL (NDC 76329-3318-1) due to lack of sterility assurance.
FDA•MODERATECytal Wound Matrix 2-Layer 5x5 cmCytal Wound Matrix 2-Layer 5x5 cm recalled over out-of-specification endotoxin results.
5 products
FDA•MODERATEReact Health PHOENIX 5L Oxygen ConcentratorReact Health PHOENIX 5L Oxygen Concentrator recalled due to devices not meeting quality specifications.
FDA•MODERATEElegance Anterior Cervical PlatesClariance-SAS is recalling Elegance Anterior Cervical Plates due to the presence of burrs on the finished product.
2 products
NHTSA•MODERATEFord Maverick and Bronco Sport Engine Block HeaterFord is recalling 2025 Maverick and 2026 Bronco Sport vehicles with 1.5L/2.0L MPC engine block heaters that may overheat and cause fire.
2 products
NHTSA•MODERATEFord F-59 and F-53 Front Axle Hub AssemblyFord is recalling 2025–2026 F-59 and F-53 vehicles with missing front axle hub spindle nuts, risking wheel detachment and loss of control.
NHTSA•MODERATEFord F-150 Transmission Range SensorFord is recalling 2015–2017 F-150 vehicles for unexpected transmission downshift risk due to sensor signal loss.
NHTSA•MODERATEFord Bronco Transmission-Transfer Case JointFord is recalling 2021–2025 Bronco vehicles for transmission-transfer case misalignment that may cause loss of drive power or rollaway.
NHTSA•MODERATEFord Ranger Sun Visor Wiring HarnessFord is recalling 2024–2026 Ranger vehicles over sun visor wiring that may short and cause fire.
2 products
FDA•MODERATEHuons: Multiple Rx Only InjectionsHuons recalls injectable lidocaine, bupivacaine, and saline due to sterility concerns.
9 products
FDA•LOWIsland Kinetics: multiple gelsIsland Kinetics recalls hydrocortisone 1% gels (Remedy Gel, Skin Rehab, Essential Calming) due to subpotency.
3 products
FDA•MODERATEAlbuterol Sulfate Inhalation Solution 0.5%Nephron SC recalling Albuterol Sulfate Inhalation Solution (NDC 69374-330-05) due to illegible labeling.
NHTSA•MODERATEEntegra Ethos Seating Capacity LabelJayco is recalling 2025–2026 Entegra Ethos RVs with incorrect seating capacity labels that may result in unbelted passengers.
NHTSA•MODERATEHarley-Davidson Softail Rear Brake LineHarley-Davidson is recalling 2025–2026 Softail motorcycles (FLHC, FXBB, FXLRS, FXLRST) due to rear brake line contact with the BCM causing brake failure.
FDA•MODERATEFluocinonide 0.05% Cream 15gTaro recalls Fluocinonide 0.05% Cream 15g tubes due to out-of-spec viscosity.
3 products
FDA•MODERATEInstinct Plus Endoscopic Clipping DeviceWilson-Cook Medical is recalling the Instinct Plus Endoscopic Clipping Device due to a potential for the device to malfunction.
NHTSA•MODERATEKia Carnival Fuel Pipe ConnectionKia is recalling 2022–2026 Carnival vehicles for fuel leak risk at the fuel pipe connection.
NHTSA•MODERATEGenesis Fuel Pipe ConnectionGenesis is recalling GV70, G90, G80, and GV80 models over fuel leak risk at pipe connection.
NHTSA•MODERATE2026 Bentley Bentayga Tire Placard LabelBentley is recalling 2026 Bentayga vehicles with incorrect tire placard weight capacity labels.
NHTSA•MODERATENissan Cube Driver Air Bag InflatorNissan is recalling 2009-2010 Cube vehicles because the driver’s air bag inflator may detach during deployment, increasing injury risk.
FDA•MODERATEHydroPeptide Clear Alliance SerumHydroPeptide Clear Alliance Serum recalled due to benzene contamination.
4 products
FDA•MODERATECinacalcet Hydrochloride Tablets 30 mgCipla recalls Cinacalcet HCl 30 mg tablets over N-Nitroso impurity above acceptable limit.
3 products
FDA•MODERATEExchange Select Honey Lemon Cough DropsExchange Select Honey Lemon Cough Drops recalled over quality concerns from FDA inspection.
15 products
FDA•MODERATERemel Yeastone BrothRemel is recalling Yeastone Broth due to the potential for incorrect antimicrobial susceptibility testing results.
FDA•MODERATELinkBio CORE WorkstationLinkBio CORE Workstation (87-9136) may display incorrect Planning Date on Start Case menu.
- Device RecallFDA•MODERATEPhilips AneurysmFlow Software
Philips is recalling AneurysmFlow software because the MAFA ratio provides unreliable prognostic data for aneurysm treatment decisions.
FDA•MODERATEArjo Tenor Mobile Patient LiftArjo Tenor patient lifts (Models KHA1000 US, KHA1010 US) recalled for actuator failure risk causing sudden arm drop.
FDA•MODERATELanreotide Injection 120 mg/0.5 mLCipla recalls Lanreotide Injection 120 mg/0.5 mL over sterility assurance concerns.
2 products
FDA•MODERATEOmnipaque (iohexol) Injection 350 mg/mLGE Healthcare recalls Omnipaque (iohexol) Injection 350 mg/mL due to particulate matter.
2 products
NHTSA•MODERATEHonda Odyssey Side Air BagsHonda is recalling 2018–2022 Odyssey vehicles; side air bags may deploy unexpectedly due to software error.
NHTSA•MODERATEJeep Cherokee Brake System Control ModuleChrysler is recalling 2026 Jeep Cherokee vehicles for brake module failure that disables ABS and electronic stability control.
2 products
NHTSA•MODERATEThomas Built Saf-T-Liner C2 Warning Lights and Stop SignThomas Built Saf-T-Liner C2 school buses (2024–2027) may lose warning lights and stop sign due to door switch software defect.
NHTSA•MODERATEIC Bus EVSB School Bus High Voltage Disconnect SwitchInternational is recalling 2022–2027 IC Bus EVSB school buses; high voltage disconnect switch may fail to cut power.
NHTSA•MODERATEJeep Wrangler Child Seat Tether WeldsChrysler is recalling 2026 Jeep Wrangler vehicles over insufficient child seat tether welds that may reduce crash restraint.
NHTSA•MODERATENova Bus Ricon Hidden Frame WindowsNova Bus is recalling Ricon hidden frame windows due to inadequate adhesion that may cause glass detachment during a crash.
NHTSA•MODERATERam 1500/2500/3500/4500/5500 Instrument Panel DisplayChrysler is recalling 2025–2026 Ram 1500/2500/3500/4500/5500 vehicles over instrument panel display failure that hides critical safety information.
NHTSA•MODERATEEnovation Controls PowerView 700 DisplayAkron Brass is recalling PowerView 700 displays (part numbers 610-00060-080-ST/080) that may fail to power on, preventing activation of emergency lights and equipment.
FDA•MODERATEStryker Sustainability Solution Tourniquet CuffsStryker is recalling tourniquet cuffs that may detach from the bladder, preventing the device from maintaining pressure.
FDA•MODERATEImu-Tek Animal Health: 2 productsImu-Tek recalls Colostrum-5 capsules and powder due to under-processing.
2 products
FDA•MODERATEXanax XR Alprazolam 3 mg TabletsViatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.
NHTSA•MODERATELexus RC, GS, IS Fuel PumpToyota is recalling 2015–2022 Lexus RC, 2016–2020 GS, and 2022 IS vehicles over fuel pump failure risk.
NHTSA•MODERATEForest River Westbrook and Avenger Travel TrailersForest River is recalling 2026 Westbrook and Avenger travel trailers with incorrect dry weight labels that may cause overloading and crash risk.
FDA•MODERATEVancomycin HCl 1.5g in 250mL Sodium Chloride InjectionFagron recalls Vancomycin HCl 1.5g/250mL injection due to sterility concern.
5 products