CPSC•
Snooz Breez 2-in-1 Smart Bedroom Fan
Snooz is recalling Breez 2-in-1 Smart fans (BZ10, BZ02 serial numbers) due to power connector corrosion that can cause overheating and fire risk.
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FSIS•MODERATEQuality Meat Sky Ranch Marinated Beef and Pork ProductsSky Ranch Meat recalled marinated beef and pork products (1.5-lb containers, Dec 2025–Apr 2026) for undeclared sesame allergen.
4 products
FDA•MODERATEOmega-3-Acid Ethyl Esters Capsules 1 gramMajor Pharmaceuticals is recalling Omega-3-Acid Ethyl Esters Capsules 1 gram (NDC 0904-7495-06) due to failed capsule shell specifications.
FDA•MODERATEThermedx FluidSmart Urology Tube SetStryker is recalling the FluidSmart Urology Tube Set due to the distribution of nonconforming products.
FDA•Revitaderm and Tridergel Antiseptic Wound Care GelBlaine Labs is recalling Revitaderm and Tridergel antiseptic wound care gels due to potential contamination with Lysinibacillus fusiformis.
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•CRITICALOrganic Peppermint Leaf PowderPure Ground Ingredients is recalling Organic Peppermint Leaf Powder due to potential Salmonella contamination.
FDA•MODERATEHologic Selenia Dimensions Mammography SystemsHologic is recalling 15+ models of Selenia Dimensions Mammography Systems due to potential internal bolt failure.
2 products- Device RecallFDA•MODERATEMedtronic SynchroMed Flex Infusion Mode A810 App
Medtronic is recalling the A810 software app for SynchroMed pumps due to a display error that can disrupt the programmed infusion schedule.
2 products 
FDA•MODERATESwan-Ganz CathetersBecton, Dickinson and Company is recalling 15+ models of Swan-Ganz Catheters due to a risk of hub leakage or breakage.
3 products
FDA•MODERATEBulk Horchata PowderMarquez Brothers International is recalling Bulk Horchata Powder due to undeclared milk, which poses a risk to those with milk allergies.
3 products
FDA•MODERATEAlendronate Sodium Oral Solution 70 mg/75 mLHikma is recalling Alendronate Sodium Oral Solution 70 mg/75 mL (NDC 0054-0282-59) due to out-of-specification assay results.
FDA•MODERATEBD GasPak EZ Gas Generating Pouch SystemsBecton Dickinson is recalling BD GasPak EZ CO2 and Campy Gas Generating Pouch Systems due to insufficient carbon dioxide production.
2 products
FDA•LOWCVS Lidocaine Wound GelCVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
FDA•DTF Sexual ChocolateNalpac is recalling DTF Sexual Chocolate due to the presence of undeclared pharmaceutical ingredients sildenafil and tadalafil.
FSIS•MODERATEWalmart Great Value Dino Shaped Chicken Nuggets — RetractionFSIS retracts alert for Walmart Great Value Dino Nuggets (Feb 10 2027) after confirming no lead contamination.
FDA•MODERATEClaravis (isotretinoin capsule, USP) 10 mgTeva is recalling Claravis 10 mg capsules (NDC 0555-1054-56, 0555-1054-86) due to out-of-specification Tretinoin impurity levels.
3 products
FDA•CRITICALKirkland Signature Traditional MadeleinesKirkland Signature Traditional Madeleines are recalled due to undeclared hazelnut and soy lecithin.
FDA•MODERATEDelflex Peritoneal Dialysis SolutionFresenius Medical Care is recalling Delflex Peritoneal Dialysis Solution due to potential bag leaks and a lack of sterility assurance.
2 products
FDA•MODERATEQuickVue Dipstick Strep A TestQuidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
FDA•MODERATELVIS Intraluminal Support DeviceMicroVention recalls LVIS Intraluminal Support Devices (REF 214022-CAS, 214518-CAS, 213517-CAS) due to dimensional nonconformance risking vessel injury or thrombosis.
FDA•MODERATELiquid Blenz Soursop BittersLiquid Blenz Soursop Bitters are recalled due to potential Clostridium botulinum contamination and unauthorized health claims.
13 products
FDA•MODERATEDakota Honey Company Spreadable Spun HoneyDakota Honey Company is recalling Original Spreadable Spun Honey due to potential contamination with stainless steel or plastic foreign objects.
5 products
FDA•Wawa Iced Tea and Lemonade DrinksWawa is recalling 16 oz Iced Tea and Lemonade drinks due to an undeclared milk allergen.
FDA•MODERATEDePuy Synthes Attune Revision Hinge Femoral ComponentDePuy Synthes is recalling the Attune Revision Hinge Femoral component due to a potential loss of sterility from packaging defects.
9 products
FDA•MODERATEFain's Blackberry Honey SpreadWalker Honey Co. is recalling Fain's Blackberry Honey Spread due to potential stainless steel or plastic particle contamination.
10 products
FDA•MODERATELundberg Family Farms Jasmine White RiceLundberg Family Farms is recalling 32 oz Jasmine White Rice due to potential foreign material contamination.
FDA•MODERATEGrace Medical Stapes ProsthesisGrace Medical is recalling the Titanium/Fluoroplastic Piston Stapes Prosthesis due to incorrect functional length listed on the labeling.
- Food RecallFDA•Karns Foods Mini Dark Chocolate Raspberry Cups
Karns Foods is recalling Mini Dark Chocolate Raspberry Cups due to undeclared peanut allergens.
CPSC•Coluans Christmas Light-Up RingsColuans Christmas Light-Up Rings (model SJP-50) recalled for accessible button cell batteries posing serious ingestion hazard to children.
CPSC•Beestech Spiral Children's Tower ToyBeestech spiral tower toy (model Bee-210316-01) recalled for choking hazard; violates small ball ban for children under 3.
CPSC•Granitestone Diamond Pro Blue Stainless Sauté PansE Mishan recalls Granitestone Diamond Pro Blue sauté pan sets (UPC 0-80313-08131-6) due to detachable metal cap that can eject when heated, causing impact and burn hazards.
CPSC•TecFlox Minoxidil Topical Solution BottlesTecFlox is recalling Minoxidil Topical Solution bottles lacking child-resistant packaging, posing poisoning risk to children.
CPSC•HTRC and Haisito T400 Battery ChargersHTRC and Haisito T400 battery chargers can ignite, posing a fire hazard and risk of serious injury or death.
CPSC•ELENKER Portable Bed RailsELENKER portable bed rails (models HFK-5115, HFK-5116, HFK-5124) recalled for entrapment and asphyxiation risk; lack required safety labels.
CPSC•Ocun Condor HMS Triple CarabinerOcun is recalling Condor HMS Triple Carabiners (batches 24003xx–25006xx) due to gate malfunction risk causing falls.
CPSC•Universal Broadmoor Canopy Bed FramesSamson International recalls Universal Broadmoor canopy bed frames (models M24109230, M24109240, M24107230, M24107240) due to collapsing canopy beams.
CPSC•Member's Mark Children's Pajama SetsSam's Club recalls Member's Mark children's pajama sets (sizes XS–XL) for violating flammability standards and posing burn hazard.
CPSC•Tuymec Minoxidil Hair Growth Spray BottlesTuymec Minoxidil Hair Growth spray bottles lack required child-resistant packaging, posing poisoning risk to children.
CPSC•Gavoyeat Halloween Light-Up RingsGavoyeat Halloween Light-Up Rings recalled for accessible button cell batteries posing serious ingestion hazard to children.
CPSC•Sangohe Adult Portable Bed RailsSangohe bed rails models 504E and 504Q recalled for entrapment and asphyxiation risk; sold on Amazon August 2023–February 2026.
FDA•MODERATEReadyMeals Turkey Bacon & Cheddar Pretzel Duo SandwichReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich is recalled due to undeclared sesame.
FDA•MODERATESterile Water for Injection USPB. Braun is recalling 3000 mL Sterile Water for Injection USP bags distributed nationwide due to potential sterility and leakage issues.
4 products
FDA•LOWAmprol 25% Medicated ArticleHuvepharma is recalling one bag of Amprol 25% medicated article due to missing lot number and expiration date information.
FDA•MODERATELidocaine HCl Injection 1% 5 mL VialsHuons is recalling Lidocaine HCl injection 1% 5 mL vials due to a lack of assurance of sterility.
9 products
FDA•CRITICALEnoki MushroomsHemu Trading is recalling 150g packages of Enoki Mushrooms due to potential Listeria monocytogenes contamination.
FDA•MODERATEepoc BGEM BUN Test CardSiemens is recalling epoc BGEM BUN Test Cards due to the risk of inaccurate pH and carbon dioxide results that may lead to improper treatment.
FDA•MODERATEPhilips Bridge Prep KitMerit Medical Systems is recalling the Philips Bridge Prep Kit due to potential catheter resistance during use.
4 products
FDA•CRITICALCook Centimeter Sizing CatheterCook is recalling Centimeter Sizing Catheters due to a risk of marker band breakage, which may cause vessel injury or life-threatening harm.
3 products
FDA•MODERATEda Vinci X and Xi Surgical System Universal Surgical ManipulatorIntuitive Surgical is recalling USM arm sub-assemblies for da Vinci X and Xi systems due to a risk of internal screw breakage.
2 products