NHTSA•MODERATE
Kumho Solus TA11 Tire
Kumho is recalling Solus TA11 tires (225/60R16) due to potential tread separation and crash risk.
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NHTSA•MODERATEAudi Q8, A7, A6 Lane Departure Warning SystemAudi is recalling 2019 Q8, A7, A6 vehicles; lane departure warning may be deactivated due to software error.
FDA•LOWCipla: Multiple Packaged In Cartons CapsulesCipla recalls Nilotinib 150 mg and 200 mg capsules over failed specification tests.
2 products
FDA•MODERATEMidodrine Hydrochloride Tablets, USP 5 mgMajor Pharmaceuticals is recalling Midodrine Hydrochloride Tablets 5 mg (NDC 0904-6818-06) due to inadequately sealed blister packaging.
FDA•MODERATEOlympus Single Use Biopsy ValveOlympus is recalling the MAJ-210 single use biopsy valve due to the potential for rubber fragments to detach during use.
2 products- Device RecallFDA•MODERATEDatascope CS300 IABP
Datascope is updating the Instructions for Use for the CS300 IABP (software version C.01) to correct battery runtime and cycle specifications.
2 products 
FDA•MODERATESTA Liatest Free Protein S KitDiagnostica Stago is recalling the STA Liatest Free Protein S kit due to potential underestimation of protein S levels in normal plasma.
NHTSA•MODERATEFord EGR ValveFord is recalling 2025 Ranger, Nautilus, Mustang, Maverick, Explorer, Escape, Corsair, Bronco Sport, and Bronco vehicles over EGR valve failure causing loss of drive power.
NHTSA•MODERATEFord Bronco and Edge Accessory Protocol Interface ModuleFord is recalling 2021–2026 Bronco and 2021–2024 Edge vehicles; APIM overheating may disable rearview camera display.
NHTSA•MODERATEFord Escape, Corsair, Aviator, Explorer Rearview CameraFord is recalling Escape, Corsair, Aviator, and Explorer vehicles (2020–2024) for inverted rearview camera images that reduce rear visibility.
NHTSA•MODERATEFord Explorer Passenger-Side HeadlightFord is recalling 2025–2026 Explorer vehicles; passenger-side headlight may turn incorrectly in curves, increasing crash risk.
NHTSA•MODERATEFord Explorer, Escape, Aviator, Corsair Windshield Wiper MotorFord is recalling 2020–2022 Explorer, Escape, Aviator, and Corsair vehicles for windshield wiper motor failure that may reduce visibility.
NHTSA•MODERATEFord F-250 SD and F-350 SD DriveshaftFord is recalling 2026–2025 F-250 SD and F-350 SD vehicles over driveshaft separation risk.
NHTSA•MODERATEFord E-350 and E-450 Backup Alarm ConnectorFord is recalling 2026–2027 E-350 and E-450 vehicles; backup alarm connector may detach, silencing the reversing alert.
NHTSA•MODERATELincoln Navigator Driver's SeatFord is recalling 2026 Lincoln Navigator vehicles due to driver's seat reversing unexpectedly at low speeds.
FDA•MODERATEACME UNITED: multiple drugsAcme United is recalling 22 varieties of BZK Antiseptic Towelettes due to manufacturing process deviations.
22 products
FDA•MODERATESemaglutide Bulk APIHarbin Jixianglong recalls semaglutide bulk API over CGMP validation failures.
2 products- Device RecallFDA•MODERATEB. Braun 21G Winged Infusion Set
B. Braun recalls 21G winged infusion sets due to risk of dull or broken needle tip.
3 products 
FDA•MODERATEAesculap Minop TrocarAesculap is recalling the Minop Trocar 150mm because the shaft may be too long.
FDA•MODERATEAtellica CH Urine Albumin TestSiemens is recalling Atellica CH Urine Albumin tests (Material 11537225) due to falsely depressed results in high-concentration samples.
FSIS•MODERATEPunahele Jerky Beef CrispsPunahele Jerky beef crisps recalled for undeclared soy allergen; best by 2/17/2027 or prior.
4 products
FDA•MODERATESavannah Bee Honey BBQ Sauce MustardSavannah Bee Honey BBQ Sauce "Mustard" bottles may contain "Sweet" sauce with undeclared wheat and soy.
FDA•MODERATETeva Pharmaceuticals: multiple tabletsTeva recalls Metoprolol Succinate ER tablets (25-200 mg) over failed dissolution specs.
4 products
FDA•CRITICALImpella RP Flex with SmartAssistAbiomed recalls Impella RP Flex with SmartAssist due to sensor drift risk.
3 products
FDA•MODERATECobas Pro Integrated Solutions Analytical UnitsRoche is recalling Cobas Pro analytical units due to a software defect that can cause the system to report erroneous, repeated test results.
2 products
FDA•MODERATEGE Healthcare Centricity Universal ViewerGE Healthcare is recalling Centricity Universal Viewer software due to a risk of patient information and image mismatch.
FDA•CRITICALFish Ball: 3 Pieces Per PiecesKOI fish balls are being recalled because they contain undeclared wheat and sesame, which are allergens and pose a risk to people with wheat or sesame allergies.
3 products
FDA•MODERATEOctopus Nuvo Tissue StabilizerMedtronic is recalling Octopus Nuvo Tissue Stabilizer (TSMICS1) due to incorrect tubing assembly that may affect surgical tissue stabilization.
FDA•MODERATECampy CVA MediumRemel is recalling Campy CVA Medium (R01272) due to low recovery of Campylobacter Jejuni on identified lots.
FDA•MODERATEAgiliti Adapt PumpAgiliti is recalling the Adapt Pump (model 61600200) for a software failure that prevents the Microclimate Management function from restarting.
NHTSA•MODERATEAcura ZDX and Prologue Instrument Panel and Rearview Camera DisplayHonda is recalling 2024 Acura ZDX and Prologue vehicles for instrument panel display failure and rearview camera blank-screen defects that increase crash risk.
NHTSA•MODERATEBMW S 1000 RR Turn SignalBMW is recalling the 2026 S 1000 RR motorcycle due to turn signal malfunction that increases crash risk.
NHTSA•MODERATEBuick Regal Rear Toe LinkGM is recalling 2012–2013 Buick Regal Turbo and GS models over rear toe link fracture risk that may cause loss of vehicle control.
NHTSA•MODERATEGeneral Motors Multiple Models Electronic Owner's ManualGM recalling 2025–2027 Chevrolet, Cadillac, GMC, and Buick models over missing electronic owner's manual.
NHTSA•MODERATEIC Bus CESB School Bus Brake LinesInternational is recalling 2023–2027 IC Bus CESB school buses; brake lines may leak due to incorrect hardware installation.
FDA•MODERATEPure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep ResetPure Solutions recalling 1 fl oz sleep formula bottles due to undeclared milk allergen from bovine colostrum.
NHTSA•MODERATEEvenflo LiteMax Factory Select Child SeatEvenflo LiteMax Factory Select (model CS100111198) recalled for incorrect weight/height limits in Spanish manual.
NHTSA•MODERATEToyota Corolla Headlight AssemblyToyota is recalling 2026 Corolla vehicles with missing headlight aim markings that may reduce visibility or create glare.
FDA•CRITICALIQF BlueberriesOregon Potato Company is recalling IQF blueberries in 30 lbs. cases and 1400 lbs. totes due to potential Listeria monocytogenes contamination.
FDA•MODERATEMedline Apheresis and Dialysis KitsMedline is recalling kits containing Tego Connectors due to potential silicone seal defects that may cause fluid leakage or therapy delays.
6 products
FDA•MODERATEEncore Medical Knee and Shoulder ImplantsEncore Medical is recalling EMPOWR 3D Knee and RSP Humeral Socket implants due to incorrect labeling.
3 products
FDA•MODERATEPIE PAK Trolley SystemEdermy is recalling PIE PAK trolley systems (models P2HC-A, P2HC-S, P2HC) due to a lack of required 510(k) clearance.
2 products
NHTSA•MODERATENewmar Bay Star Hood StopNewmar is recalling 2018–2026 Bay Star motorhomes; hood stop adhesive may fail and detach during transit.
NHTSA•MODERATENewmar Freedom Aire Hydronic Heating SystemNewmar is recalling 2026 Freedom Aire motorhomes; hydronic heating system may unintentionally activate and produce harmful gas.
NHTSA•MODERATEThomas Built Buses Saf-T-Liner C2 Heater HoseDTNA is recalling 2027 Thomas Built Buses Saf-T-Liner C2 school buses over heater hose rupture risk and hot coolant leaks.
FDA•LOWEptifibatide Injection 75 mg/100 mLSlate Run Pharmaceuticals recalls Eptifibatide Injection 75 mg/100 mL vials (NDC 70436-027-80, 70436-163-80) due to incorrect dosing-route labeling.
FDA•MODERATEAmantadine HCl Capsules 100 mgAvKARE is recalling Amantadine HCl Capsules 100 mg (NDC 50268-069-15) nationwide due to failed dissolution specifications.
FDA•MODERATEAdbry (tralokinumab-ldrm) InjectionLEO Pharma is recalling Adbry (tralokinumab-ldrm) injection due to a lack of sterility assurance following the discovery of wool fiber.
NHTSA•CRITICALSubaru Crosstrek Hybrid and Forester Hybrid Fuel CapSubaru is recalling 2026 Crosstrek hybrid and 2025 Forester hybrid vehicles over fuel cap seal defect that may cause fuel leakage and fire risk.
NHTSA•MODERATEKia Telluride Front Seat Back FrameKia is recalling 2025 Telluride vehicles with power front seats due to seat back frame failure risk in crashes.