FDA•MODERATE
AMS DSAEK Pack Convenience Kit
Windstone recalls AMS DSAEK Pack kits (Part AMS12394B) due to detached blue BOPs in saline bags.
Filters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
FDA•MODERATEMedicaLyte Liquid Bicarbonate ConcentrateNipro recalls MedicaLyte hemodialysis concentrate (REF BC-100, BC+201) over high endotoxin levels.
4 products- 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•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.
NHTSA•MODERATERenegade RV MaxxAir Maxxfan PCBKibbi recalls Renegade RVs with MaxxAir Maxxfan rooftop fans: PCB may overheat, posing a fire risk.
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•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.
- 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
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•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.
FDA•MODERATEMedline Convenience KitsMedline recalls two convenience kits over sterility breach risk in included BD ChloraPrep and FREPP applicators.
16 products
NHTSA•MODERATEBlue Bird Vision Wheelchair LiftBlue Bird recalls Vision school buses with Ricon K-Series wheelchair lifts due to contactor failure that may cause unintended movement.
NHTSA•MODERATEEntegra Qwest and Jayco Melbourne Prestige Taillight HarnessJayco recalls 2027 Entegra Qwest and Melbourne Prestige RVs over a taillight harness resistor defect.
NHTSA•MODERATEEntegra Accolade and Jayco Seneca Certification LabelJayco recalls certain 2026-2027 Entegra Accolade and Jayco Seneca RVs over incorrect tire size on certification labels.
NHTSA•MODERATETiffin Wayfarer LP TankTiffin recalls 2026-2027 Wayfarer RVs: LP tank may lack remote shut-off and be loose, posing fire and crash risks.
FDA•MODERATEPrasugrel Tablets 10mgMylan recalls Prasugrel Tablets 10mg over failed dissolution specs.
FDA•MODERATETHE ONE SPF 50 Invisible Sunscreen GelAllies Group recalls THE ONE SPF 50 Invisible Sunscreen Gel over subpotent protection.
4 products
FDA•MODERATEWeis Pasteurized Apple CiderWeis Markets recalls Fresh From the Orchard pasteurized apple cider over high patulin levels.
FDA•LOWDoxylamine Succinate and Pyridoxine HCl Delayed-Release TabletsBionpharma recalls Doxylamine Succinate and Pyridoxine HCl 10 mg/10 mg tablets over foreign tablets or capsules.
FDA•MODERATESTA Staclot Protein SDiagnostica Stago recalls STA Staclot Protein S reagent over QC drift within its 4-hour stability period.
FDA•MODERATEBaxter Healthcare: multiple drugsBaxter recalls 17 sterile injectable drugs, including Vancomycin and Clindamycin, over CGMP deviations.
17 products