FSIS•CRITICAL
Imported Pork Guanciale
Prime Line Distributors and Ferrarini USA recall imported RTE pork guanciale over possible Listeria contamination.
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FDA•LOWAfricando Alfredo Hot SauceAfricando Alfredo Hot Sauce recalled for undeclared wheat and soy allergens.
NHTSA•CRITICALBell Pit Boss HelmetsBell is recalling certain Pit Boss helmets (size medium, 2025-2026) over inadequate impact protection, violating FMVSS 218.
FDA•CRITICALTyenne (tocilizumab-aazg) Injection 400 mg/20 mLFresenius Kabi recalls Tyenne ( (tocilizumab-aazg) 400 mg/20 mL vials over glass particles.
FDA•CRITICALGet Fresh Produce Jalapeno PeppersGet Fresh Produce recalls jalapeno peppers over potential Salmonella contamination.
FDA•CRITICALENROUTE Transcarotid Neuroprotection SystemBoston Scientific recalls ENROUTE Transcarotid Neuroprotection System over sheath tip separation risk.
2 products
NHTSA•CRITICALLucid Air Exterior Lighting CircuitLucid is recalling certain 2022-2026 Air vehicles over an exterior lighting circuit that may overheat, posing fire and crash risks.
FDA•CRITICALLactated Ringer's Injection USP 1000 mLB. Braun recalls Lactated Ringer's Injection 1000 mL over particulate matter.
FDA•CRITICALCoast Tropical Jalapeno PeppersCoast Citrus recalls bulk jalapeno peppers over potential Salmonella Javiana contamination.
FSIS•CRITICALGangothri Pickled Goat and ChickenGangothri Foods recalls 1,626 lbs of RTE pickled goat and chicken products made without inspection.
4 products
FDA•CRITICALLacnola Small Batch Lactation GranolaLacnola Lactation Granola recalled over possible Salmonella contamination.
FDA•LOWParagon 28 Navicular Cage Foot ImplantParagon 28 recalls Navicular Cage foot implant (Model 6123S R) due to elevated oxygen levels.
2 products
FDA•CRITICALWhole Foods: Guacamole and Salsa DipsWhole Foods recalls guacamole and salsa dips over possible Salmonella from jalapenos.
10 products
FDA•CRITICALBaxter Duo-Vent Solution SetBaxter recalls Duo-Vent Solution Set (1C8507) over air bubble risk in drip chamber and tubing.
FDA•CRITICALMorphine Sulfate Injection 2 mg/mL Prefilled SyringesFresenius Kabi recalls Morphine Sulfate 2 mg/mL syringes over a label mixup that may contain Dilaudid.
2 products
FSIS•CRITICALMidamar Beef Pastrami and Corned Beef BrisketCity Foods recalls 3,215 lbs of RTE pastrami and corned beef over Listeria risk; EST. 1896.
3 products
FSIS•CRITICALAl Kabeer Breaded Swai Fish Fillets and SticksShan Distribution recalls 5,084 lbs of Al Kabeer breaded Swai fish fillets and sticks due to import violation.
3 products
FDA•CRITICALGarden Salad 7.75 ozCibus Fresh, Sprig & Sprout, and Jack & Olive Garden Salad 7.75 oz recalled for possible Cyclospora contamination.
NHTSA•CRITICALIsuzu NPR HD Liftgate Deck PinsUS Truck Body recalls 2025 Isuzu NPR HD liftgates: deck pins may break, causing platform to fall.
FDA•CRITICALGlutathione 200 mg/mL InjectionVictory Medical Center Pharmacy recalls Glutathione 200 mg/mL vials over bacterial endotoxin contamination.
FDA•CRITICALKC Everyday Mac & CheeseKerry recalls KC Everyday Mac & Cheese over undeclared egg allergen.
FDA•LOWSyva Emit Tox Tricyclic Antidepressant Calibrator/ControlsSiemens recalls Syva Emit Tox Tricyclic Antidepressant Calibrator/Controls due to out-of-specification sodium azide concentration.
FDA•LOWSyva Emit Disopyramide AssaySiemens recalls Syva Emit Disopyramide Assay due to out-of-spec sodium azide concentration; risk of mild irritation.
FDA•CRITICALOptiray 350 Ioversol InjectionLiebel-Flarsheim recalls Optiray 350 Ioversol Injection 500 mL vials due to particulate matter (plastic, steel, glass).
2 products
FDA•CRITICALHalyard Cardiac Cath Pack with Medline ManifoldAVID Medical recalls Halyard kits with Medline manifolds due to particulate risk.
3 products
FDA•CRITICALBD Needle Kit for Powered DriverBard Access recalls BD Powered Driver Needle Kits over obturator removal difficulty.
NHTSA•CRITICALWinnebago Ekko Motorhome GeneratorWinnebago recalls 2024-2025 Ekko motorhomes: touchscreen may turn on generator, risking CO poisoning.
FDA•CRITICALAquafaba Powder529 Commerce recalls Aquafaba Powder over undeclared egg allergen.
FDA•CRITICALResmed Astral 100/150 VentilatorResMed recalls Astral 100/150 ventilators due to supercapacitor leakage that may interrupt ventilation.
FDA•CRITICALRelax 5-HTP Plus Vitamin B6Relax 5-HTP Plus Vitamin B6 recalled for elevated 5-HTP levels above allowed dosage.
2 products
FDA•CRITICALCefazolin in Dextrose InjectionBaxter recalls Cefazolin in Dextrose 2g/100mL infusion bags due to particulate matter.
FDA•CRITICALAmerican Regent: Multiple Packaged In InjectionsAmerican Regent recalls Nitroglycerin Injection 50 mg/10 mL and other injectables due to particulate matter (hair).
14 products
FDA•LOWAscend Laboratories: Multiple Dabigatran Etexilate CapsulesAscend recalls Dabigatran Etexilate 75mg/150mg capsules over impurity spec failures.
6 products
NHTSA•CRITICALK&N and Spectre Fuel Filter O-RingK&N recalls fuel filters with O-ring that may disintegrate, causing fuel leak and fire risk.
FDA•CRITICALMedline Anterior Hip KitMedline is recalling anterior hip kits containing Bupivacaine Hydrochloride in Dextrose Injection over quality issues.
4 products
FDA•CRITICALMedline HIP CDS-LF KitMedline is recalling specific lots of procedure kits containing Bupivacaine ampules due to a quality issue that could cause drug ineffectiveness.
4 products
FDA•CRITICALCetirizine Hydrochloride Tablets 5 mgRising Pharma recalls Cetirizine HCl 5 mg tablets due to ranitidine cross-contamination.
FDA•CRITICALTaylor Farms de Mexico S. de: 21 productsTaylor Farms recalls 21 lettuce products over Cyclospora risk.
21 products
FDA•LOWTrokendi XR Topiramate ER Capsules 25mgSupernus recalls Trokendi XR 25mg capsules over failed dissolution specs.
3 products- FDA•LOWAscend Laboratories: Multiple Dabigatran Etexilate Capsules
Ascend recalls Dabigatran etexilate capsules (110 mg, 150 mg) over impurity test failures.
2 products 
NHTSA•CRITICALInternational MV and HV Battery Interconnect CableInternational is recalling certain MV and HV vehicles because the battery cable may short circuit, posing a fire risk.
FDA•CRITICALTransvenous Pacing Electrode TrayArgon recalls Transvenous Pacing Electrode Trays due to non-sterile lidocaine ampules in kits.
6 products
FDA•CRITICALAbiomed Impella RP Flex IntroducerAbiomed recalls Impella RP Flex introducers over sheath leakage risk.
13 products
NHTSA•CRITICALBMW Engine Starter RelayBMW is recalling certain 530e, 740Le, and 330e iPerformance vehicles due to an engine starter relay that may corrode and cause a fire.
FDA•CRITICALReprocessed Electrophysiology and Ultrasound CathetersMedline is recalling reprocessed catheters due to residual particulate matter that may cause infection or embolism.
FDA•CRITICALMedtronic Harmony Delivery Catheter SystemMedtronic is recalling the Harmony Delivery Catheter System due to a manufacturing defect that may cause the distal tip to detach during use.
NHTSA•CRITICALKia Telluride Power Seat MotorKia is recalling 2020-2024 Telluride vehicles due to a risk of fire from overheating front power seat motors.
NHTSA•CRITICALHyundai Ioniq 5 High Voltage BatteryHyundai is recalling 2023-2024 Ioniq 5 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.
NHTSA•CRITICALKia EV6 and EV9 High Voltage BatteryKia is recalling 2022-2024 EV6 and 2024 EV9 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.
NHTSA•CRITICALCrestline Ford CCL166 Type III Emergency VehicleCrestline is recalling 2026 Ford CCL166 Type III emergency vehicles due to a fuel line puncture risk that may cause a fire.