CPSC•
Member's Mark 7' Pre-Lit Twinkling Buck
Member's Mark 7' Pre-Lit Twinkling Buck (model 990404199) recalled over burn hazard from resistor overheating.
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CPSC•Maitys Magnetic Drinkware CharmsMaitys magnetic drinkware charms (400-piece sets) contain loose magnets posing serious ingestion hazard to children.
CPSC•VEEKTOMX VT103 Mini Power BanksVEEKTOMX VT103 mini power banks sold on Amazon (Jan–Sep 2024) recalled for fire and burn hazards from overheating lithium-ion batteries.
CPSC•Male-to-Male Extension Cords (Pigtail Cables)Shenzhen Shijingjie is recalling male-to-male extension cords (models RY-US-06, RY_US-1.5) sold on Walmart over electrocution and carbon monoxide poisoning risks.
CPSC•Vitaquest International Iron Supplement Bottles and PacketsVitaquest is recalling 11 brands of iron supplements (Arey, Bari Life, Bird&Be, Biote, Dr. Fuhrman, NuLife, HMR, Bariatric Pal, Noevir, Zenbean, Sakara) with non-child-resistant packaging.
CPSC•ShymeryDirect LED LightsShymeryDirect LED lights with accessible CR2032 coin batteries pose ingestion hazard to children; can cause serious injury or death.
CPSC•Wybotics Robotic Pool VacuumsWybotics is recalling Osprey 700 Max and S1 robotic pool vacuums over lithium-ion battery overheating risk.
CPSC•Yeeluzan Pool Drain CoversYeeluzan pool drain covers violate federal entrapment safety standards, posing drowning risk.
CPSC•Silks Children's Loungewear SetsSilks is recalling children's loungewear sets (sizes 2T–13/14) sold online January 2024–September 2025 due to flammability standard violations and burn hazard risk.
CPSC•Snooz Breez 2-in-1 Smart Bedroom FanSnooz is recalling Breez 2-in-1 Smart fans (BZ10, BZ02 serial numbers) due to power connector corrosion that can cause overheating and fire risk.
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•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•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
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•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•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.
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•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•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•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
FDA•MODERATEOne Step 10A In Vitro Diagnostic TestDFI is recalling the One Step 10A in vitro diagnostic test because it was distributed without required FDA premarket clearance or approval.
7 products