CPSC•
BAYOTAK USA Electric Pressure Washers
BAYOTAK USA pressure washers (model C4012PLUS-1500C) lack GFCI protection, posing electrocution risk.
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CPSC•LED Finger Beam Lights Model A10-8ZMC Group recalls LED Finger Beam Lights (model A10-8) with accessible button cell batteries that pose serious injury or death risk if swallowed.
CPSC•Arch Studio Tea KettleArch Studio tea kettles (model HJ10525) recalled due to detachable handle burn hazard.
CPSC•Sanlebi Pet Vet PlaysetSanlebi Pet Vet Playset (model MX094) recalled for easily accessible button cell batteries in toy tools; risk of serious injury from ingestion.
CPSC•SpringFlower 5-in-1 Montessori Toy SetSpringFlower 5-in-1 Montessori Toy Set (model SFTODD05IN1) recalled for choking hazard from airplane teething toy with tentacle ends.
CPSC•SEGMART 55" Mini Round Toddler Trampolines with Accessory KitsSEGMART recalls 55" toddler trampolines with accessory kits (models SOSTT051BR, SOSTT051CR, SOSTT051YP) due to strangulation hazard from hammock and accessory straps.
CPSC•Sweetcrispy Pressure WashersSweetcrispy model XCJ-K01 pressure washers lack GFCI protection, posing shock and electrocution risk.
FDA•MODERATENegita Cracker ShrimpHadson is recalling Negita Cracker Shrimp 2.8 oz over undeclared FD&C Yellow 6.
FDA•MODERATEPublix Bran FlakesPublix Bran Flakes are being recalled due to the potential presence of plastic foreign material.
FDA•CRITICALBreeder's Edge Foster Care Puppy Milk ReplacerBreeder's Edge is recalling various sizes of Puppy Milk Replacer due to inconsistent vitamin D levels.
2 products- Food RecallFDA•MODERATESilver Moon LP: 48 recalled products
48 Silver Moon LP products recalled over tree nuts, peanuts, milk, eggs, soy, wheat, sulfites, and other hazards.
48 products 
FDA•MODERATECovidien Shiley Tracheostomy TubeCovidien is recalling Shiley Tracheostomy Tubes (REF 6FEN) due to incorrect display box labeling.
FDA•MODERATECovidien EndoStitch Polysorb Single Use Loading UnitCovidien is recalling EndoStitch Polysorb loading units (models 170053 and 170071) due to a compromised sterile barrier.
FDA•MODERATEPhilips Achieva 1.5T MR Elastography SystemPhilips is recalling Achieva 1.5T MRE systems due to a software error that may cause inaccurate stiffness value measurements.
19 products
FDA•MODERATESpecially SELECTED Vanilla Creme BruleeLactalis Canada is recalling Specially SELECTED Vanilla Creme Brulee (3.6 oz) over possible glass contamination.
FDA•MODERATEDexcom G7 CGM iOS AppDexcom is recalling G7 CGM iOS app versions 2.9.0–2.11.2 due to a software defect that may delay glucose alerts and readings.
4 products
FDA•MODERATE52USA Strawberry Popping Boba52USA Strawberry Popping Boba is recalled for containing unapproved food colors including FD&C Yellow 5, Yellow 6, and Red 40.
6 products
FDA•MODERATEPhysio-Control LIFEPAK DefibrillatorsPhysio-Control is recalling various LIFEPAK defibrillators due to missing documentation of required performance inspections.
FDA•MODERATELUCAS Chest Compression SystemJolife AB is recalling LUCAS 2, 3, and 3.1 chest compression systems due to missing service documentation.
2 products
FDA•MODERATESwad Orange Flavored Masala CandyRaja Foods is recalling Swad Orange Flavored Masala Candy due to undeclared FD&C Yellow 6.
2 products
FDA•MODERATEHalyard Purezero Ultraviolet Nitrile Exam GlovesHalyard is recalling Purezero Ultraviolet Nitrile Exam Gloves due to a failure to meet chemical permeation performance specifications.
FDA•MODERATECodman CerebroFlo EVD CatheterIntegra LifeSciences is recalling the CerebroFlo EVD Catheter due to out-of-specification endotoxin results.
FDA•CRITICALArrow Edge Hemodialysis Catheterization Kit Sheath IntroducerArrow is recalling hemodialysis kits containing a defective sheath introducer that may fail to split, risking injury during procedures.
6 products
FDA•MODERATEBard Dynamic Deca Steerable Electrophysiology CatheterStryker is recalling Bard Dynamic Deca Steerable Electrophysiology Catheters due to incomplete sterile packaging seals.
26 products
FDA•MODERATEMedline Eye Tray-LF Convenience KitMedline is recalling Eye Tray-LF kits containing mislabeled Cardinal Health syringes that may lead to incorrect insulin dosing.
FDA•CRITICALMedline Anesthesia TraysMedline is recalling anesthesia trays containing Huons Bupivacaine due to quality concerns, data integrity issues, and reduced efficacy.
7 products
CPSC•BISSELL Steam Shot OmniReach Steam CleanersBISSELL recalls 1M+ Steam Shot OmniReach steam cleaners (models 4155, 4171) over burn hazard from detaching attachments.
CPSC•Head Ski BootsHead is recalling ski boots with fluorescent yellow components (model years 2016–2022) due to material deterioration and fall risk.
CPSC•Besslly Halloween Pumpkin Carving KitsBesslly Halloween Pumpkin Carving Kits (Model CHD-014-2) recalled due to easily accessible button cell batteries posing ingestion hazard to children.
CPSC•Easymake Adult Portable Bed RailsEasymake adult portable bed rails pose entrapment and asphyxiation risk; violate mandatory safety standard.
CPSC•Prestige Supernova and Typhoon Butane LightersPrestige is recalling Supernova and Typhoon butane lighters lacking child-resistant mechanisms, posing fire and burn hazards.
CPSC•Happiness Light LED LightsHappiness Light recalls LED lights with accessible CR2032 coin batteries due to child ingestion hazard and missing warnings.
CPSC•SCUBAPRO Monorail Weight Pocket for BCDSCUBAPRO is recalling Monorail Weight Pockets for BCDs because the D-ring handle can detach, preventing emergency removal and creating a drowning risk.
CPSC•Muscccm Pool Drain CoversMuscccm pool drain covers violate safety standards, posing entrapment and drowning hazards.
CPSC•Member's Mark 7' Pre-Lit Twinkling BuckMember's Mark 7' Pre-Lit Twinkling Buck (model 990404199) recalled over burn hazard from resistor overheating.
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.
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•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