FDA•
0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill
B. Braun recalls 0.9% Sodium Chloride Injection, 100 mL Partial Fill, due to particulate matter (iron oxide, cellulose, polystyrene).
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FDA•MODERATEAMS DSAEK Pack Convenience KitWindstone recalls AMS DSAEK Pack kits (Part AMS12394B) due to detached blue BOPs in saline bags.
FDA•MODERATEMedicaLyte Liquid Bicarbonate ConcentrateNipro recalls MedicaLyte hemodialysis concentrate (REF BC-100, BC+201) over high endotoxin levels.
4 products
FSIS•CRITICALChicharrón Pork Crackling Potato ChipsEl Eden recalls pork crackling chips due to import violation; full variant list on FSIS page.
2 products
FDA•fentaNYL Citrate Injection 1,000 mcg/100 mLOurPharma recalls fentaNYL Citrate Injection 1,000 mcg/100 mL over mislabeled expiry dates; NDC 73013-1013-01.
FDA•Alfalfa 50 lb BagsAlfalfa 50 lb bags recalled over potential E. coli and Salmonella contamination.
- Food RecallFDA•MODERATEFannie May & XO Marshmallow Pixie S'mores Collection
Fannie May & XO Marshmallow Pixie S'mores Collection recalled for undeclared milk and pecans.
FDA•CRITICALEpidural/Pain TQC KitMedical Action recalls its Epidural/Pain TQC Kit containing sodium chloride ampules over compromised sterility.
2 products
FDA•LOWPovidone Iodine/Proparacaine Ophthalmic SolutionImprimis NJOF recalls ophthalmic solution for being subpotent, risking reduced efficacy.
FDA•LOWFluphenazine HCl Tablets 1mgAjanta Pharma recalls Fluphenazine HCl 1mg tablets (NDC 27241-255-01) due to impurity out-of-specification.
FSIS•CRITICALImported Pork GuancialePrime Line Distributors and Ferrarini USA recall imported RTE pork guanciale over possible Listeria contamination.
4 products
NHTSA•MODERATERenegade RV MaxxAir Maxxfan PCBKibbi recalls Renegade RVs with MaxxAir Maxxfan rooftop fans: PCB may overheat, posing a fire risk.
FDA•CRITICALCrown Farms Dried Suri CutEuro Foods recalls Crown Farms Dried Suri Cut (200 gm) over improper evisceration.
FDA•MODERATESoft PVC Thoracic CathetersThis recall involves thoracic catheters manufactured for use in draining fluid or air from the chest cavity.
3 products
FDA•MODERATEDermaV Laser SystemLutronic recalls DermaV Laser System over burn risk from spark/loud noise at high fluences.
FDA•MODERATEHeartSine Samaritan PadsSee the official recall notice for details about this display summary.
FDA•MODERATEHalyard IV Start KitAVID Medical recalls Halyard IV Start Kits (REF KRIV26-02) due to sterility concerns with included applicators.
FDA•Epinephrine Injection 30 mg/30 mLAmerican Regent recalls epinephrine 30 mg/30 mL vials due to glass particulates and sterility concerns.
FDA•LOWTrokendi XR (topiramate) Extended-Release CapsulesTrokendi XR (topiramate) 50 mg capsules recalled over failed dissolution specs.
FDA•MODERATEMycophenolate Mofetil for InjectionMylan recalls Mycophenolate Mofetil for injection, 500 mg/vial, over failed dissolution specs.
FDA•MODERATEBD Urinary Catheter Trays with CliniClean Pericare WipesBD Urinary Catheter Trays with CliniClean Pericare Wipes recalled over possible lubricant contamination causing skin irritation.
12 products
FDA•MODERATEGRANUFLO Dry Acid ConcentrateFresenius recalls GRANUFLO Dry Acid Concentrate (0FD2251-3B, 0FD3251-3B) over blue-green discoloration.
3 products
FDA•MODERATEtraZODone Hydrochloride Tablets, USP, 50 mgTeva recalls traZODone HCl 50 mg tablets due to foreign tablets/capsules in product.
FDA•MODERATEFresenius 5008X Blood Tubing SetFresenius recalls 5008X blood tubing set (PN 03-5110-6) over blood leak risk.
4 products
FDA•MODERATEDiscofix Four Way StopcockB Braun recalls Discofix Stopcock Sets over incorrect expiration date on carton label.
- Device RecallFDA•MODERATELUX-Dx Insertable Cardiac Monitor System Software
Boston Scientific recalls LUX-Dx ICM server software (Model 7260) over delayed AF Burden Alerts.
3 products 
FDA•LOWWonton Specialists: 6 productsWonton Specialist recalls noodles and dumpling skins for undeclared FD&C Red No. 40, an allergen risk.
6 products
FDA•MODERATEVelys Enabling Tech Robotic-Assist StationMedos recalls Velys Robotic-Assist Station over software issue causing unintended arm movement.
FDA•MODERATEPooled Cryoprecipitated AHFVitalant recalls Pooled Cryoprecipitated AHF for not meeting specifications.
FDA•CRITICALAddall XR ShotAddall XR Shot recalled for undeclared 1,4-DMAA, Phenylethylamine, and Phenibut.
- Vehicle RecallNHTSA•MODERATEToyota C-HR Electric Drive System Battery
Toyota recalls 2026 C-HR EVs: software error may overcharge battery, causing loss of drive power and crash risk.
- Device RecallFDA•MODERATEPhilips Brilliance CT Systems
Philips recalls Brilliance iCT and related CT systems over unintended radiation issue.
4 products 
FDA•MODERATELexia: Multiple Broadway Joe's Pain CreamsLexia LLC recalls Broadway Joe's Pain Cream over potential raw material contamination.
2 products
FDA•2% Chlorhexidine Gluconate ClothsSage Products recalls 2% Chlorhexidine Gluconate Cloths over possible cross-contamination.
NHTSA•MODERATETesla Model Y Front Suspension Lateral LinkTesla recalls 2026 Model Y over front suspension lateral link fasteners that may loosen, risking loss of control.
NHTSA•MODERATEWabash Dry Van TrailersWabash recalls dry van trailers over front corner castings that may crack and separate, increasing crash risk.
- Vehicle RecallNHTSA•MODERATELight Boy GBX12SK Light Towers
Light Boy America is recalling certain GBX12SK light towers because the trailer frame may bend at the tow bar, which could cause the light tower to detach and create a road hazard for other vehicles.
NHTSA•MODERATE2024-2025 Thomas Built Buses School Bus WindshieldsThomas Built Buses is recalling certain 2024-2025 school bus windshields that may not comply with federal motor vehicle safety standards.
NHTSA•MODERATEFord F-150 Brake HoseBrake hose may leak, causing brake loss; dealers will replace it free.
NHTSA•MODERATE2025-2026 Ram 1500 Radio SoftwareRadio software error may prevent rearview camera image from displaying.
NHTSA•MODERATEPeterbilt Truck Brake HoseSee the official recall notice for details about this display summary.
NHTSA•MODERATEJeep Grand Cherokee Rear Coil SpringsSee the official recall notice for details about this display summary.
NHTSA•MODERATEJeep TPMS Software UpdateChrysler recalls certain Jeep SUVs over TPMS software error that may fail to alert low tire pressure.
NHTSA•MODERATEStoryteller MODE/GXV HILTS Maxxfan PCBStoryteller recalls 2026-2027 MODE and 2026 GXV HILTS vehicles with MaxxAir Maxxfan rooftop fans due to PCB overheating fire risk.
FDA•Buprenorphine Sublingual Tablets 2 mgAmerican Health Packaging recalls Buprenorphine Sublingual Tablets 2 mg over a label mix-up.
FDA•MODERATEMedline Convenience Kits with BD ChloraPrep Clear 1mL ApplicatorsMedline recalls Convenience Kits with BD ChloraPrep Clear 1mL Applicators over possible open or incomplete seals.
13 products
FDA•MODERATEBaxter Novum IQ Syringe PumpBaxter recalls Novum IQ Syringe Pump over a software issue during multi-syringe infusions.
2 products
FDA•MODERATEHEALON EndoCoat PRO and DUET PRO IIJ&J Surgical Vision updates instructions for HEALON viscoelastic products used in cataract surgery over cannula insertion risks.
FDA•MODERATEApheresis Platelets, Leukocytes Reduced, IrradiatedNew York Blood Center Enterprises recalls Apheresis Platelets, Leukocytes Reduced, Irradiated units over excessive platelet count.
FDA•LOWApheresis Red Blood Cells, Leukocytes Reduced, IrradiatedNew York Blood Center recalls apheresis red blood cells over incorrect anticoagulant ratio.