FDA•MODERATE
ICU Medical Oncology Extension Set
ICU Medical is recalling Oncology Extension Set REF: CL3960 due to a potential leak that could cause therapy interruption or hazardous exposure.
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FDA•WAP Sensual Enhancement CapsulesWAP Sensual Enhancement capsules recalled for undeclared sildenafil, tadalafil, and flibanserin.
FDA•CRITICALKroger Homestyle Cheese and Garlic CroutonsKroger Homestyle Cheese and Garlic Croutons recalled over possible Salmonella from milk powder.
FDA•CRITICALPS Seasoning & Spices: 6 productsPS Seasoning recalls Ellsworth Sour Cream + Onion Seasoning and other seasonings over Salmonella risk.
6 products
FDA•MODERATEOphthavet Ophthalmic SolutionDechra is recalling Ophthavet Ophthalmic Solution for dogs and cats due to a lack of sterility assurance.
FDA•MODERATETangent Single Use Digital CatheterTangent Endoscopy is recalling single-use digital catheters due to potential fractures at the distal shaft tip.
FDA•MODERATESwan-Ganz Catheters (Multiple Models)Becton, Dickinson and Company is recalling multiple variants of its Swan-Ganz pulmonary artery catheters due to a potential risk of valve leakage that may affect the balloon inflation performance.
3 products
FDA•MODERATEStraus Family Creamery: 5 productsStraus Family Creamery recalls Organic Super Premium Ice Cream over possible metal pieces.
5 products
CPSC•Amazon Basics Adjustable DumbbellsAmazon is recalling 55 lb. adjustable dumbbells due to an impact hazard caused by weight plates that can dislodge during use.
CPSC•Can-Am Outlander Pro and Max Pro ATVsCan-Am is recalling certain Outlander Pro and Max Pro ATVs due to a speed limiter malfunction that poses a serious crash and injury risk.
CPSC•Cosyland Children's Tower StoolsCosyland is recalling children's tower stools (models CS0003 and CS0092-4) due to collapse, fall, and entrapment hazards.
CPSC•Generac and DR Power Electric Start Pressure WashersGenerac and DR Power pressure washers are recalled due to a carbon monoxide poisoning risk from a malfunctioning electric start button.
CPSC•Guidecraft Children's Standing TowersGuidecraft is recalling children's standing towers due to a fall hazard caused by a platform that can loosen and detach.
CPSC•LiCB Lithium Coin BatteriesLiCB CR2032 lithium coin batteries are recalled for lacking child-resistant packaging and warning labels, posing a severe ingestion hazard.
CPSC•Minka Bardon Series Pendant Light FixturesMinka is recalling Bardon Series pendant light fixtures because the frame can detach during installation, posing an impact hazard.
CPSC•Misco Sports Badminton Toy SetsMisco Sports badminton toy sets are recalled due to a battery ingestion hazard from easily accessible button cell batteries in the shuttlecock.
CPSC•Petzl ASTRO and CANYON GUIDE HarnessesThe full list of affected model numbers and serial ranges is available on the CPSC recall page.
CPSC•Petzl SIMBA and SWAN EASYFIT HarnessesPetzl is recalling SIMBA and SWAN EASYFIT harnesses due to a buckle defect that poses a serious fall hazard.
CPSC•Superbobi Pool Drain CoversSuperbobi pool drain covers are recalled for failing to meet safety standards, posing entrapment and drowning hazards to swimmers.
CPSC•Tiyol Pull String Teething ToysTiyol pull string teething toys (Model 688-59) are recalled due to a choking hazard from strings that can lodge in a child's throat.
CPSC•Agio Menlo Woven Patio SwingsAgio Menlo Woven Patio Swings (model 1934256) are being recalled due to a fall hazard where the seat can detach from the frame.
CPSC•Zwilling Enfinigy Electric KettlesZwilling is recalling Enfinigy electric kettles because the handle can detach, posing a burn hazard from hot contents.
FDA•MODERATEProspector Popcorn Belgian Chocolate Toffee PopcornProspector Popcorn Belgian Chocolate Toffee recalled for undeclared soy (soy lecithin).
2 products
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.
- Device RecallFDA•MODERATEMedtronic SynchroMed Flex Infusion Mode A810 Software
Medtronic is recalling A810 software for SynchroMed pumps due to a display error that may cause incorrect or missed medication delivery.
2 products 
FDA•CRITICALDOXOrubicin Hydrochloride Liposome InjectionSun Pharma recalls DOXOrubicin Liposome Injection 50 mg/25 mL vials due to glass particulate matter.
FDA•CRITICALHellas Meze Golden Smoked Whole HerringTerra Medi is recalling Hellas Meze Golden Smoked Whole Herring due to potential Clostridium botulinum contamination.
FDA•CRITICALEnoki MushroomsIQ Produce is recalling 150g Enoki Mushrooms due to potential Listeria monocytogenes contamination.
FDA•CRITICALEnoki MushroomsHH Fresh Trading is recalling 150g packages of Enoki Mushrooms due to potential Listeria monocytogenes contamination.
FDA•MODERATERaja Foods and Vegetables: 2 Flavored Masala CandiesRaja Foods recalls Swad Orange and Mango Masala Candies due to undeclared FD&C Yellow 6.
2 products
FDA•MODERATECodman CerebroFlo EVD CatheterIntegra LifeSciences is recalling the Codman CerebroFlo EVD Catheter due to out-of-specification endotoxin results.
FDA•CRITICALArrow Edge Hemodialysis Catheterization ProductArrow Edge hemodialysis catheterization product recalled: sheath introducer may not split, risking injury.
6 products
FDA•CRITICALOmnicell i.v.STATION Syringe LabelsOmnicell is recalling sterile syringe label stock for the i.v.STATION device due to a risk of mislabeled IV medication syringes.
FDA•MODERATEBARD Dynamic Deca Steerable CatheterBARD Dynamic Deca Steerable EP catheter recalled due to incomplete seals on sterile product.
26 products
FDA•MODERATEEdwards EVOQUE Tricuspid Delivery SystemEdwards Lifesciences is updating the labeling for the EVOQUE tricuspid delivery system to include a warning about potential functionality issues.
FDA•MODERATECreamy Sesame NoodlesFly By Jing recalls Creamy Sesame Noodles over possible undeclared peanut allergen.
FDA•MODERATEZYMUTEST HIA IgG ELISA KitZYMUTEST HIA IgG ELISA kit lot FD1265 distributed with outdated flyer containing incorrect positive control values.
FDA•MODERATEPhilips Azurion Cable Hose CarrierPhilips is recalling Azurion imaging systems due to potential loosening or breakage of Cable Hose Carrier bolts and plastic parts.
FDA•MODERATEQuickVue Dipstick Strep A TestQuidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
FDA•MODERATEThermedx FluidSmart Urology Tube SetStryker is recalling the FluidSmart Urology Tube Set (REF LL0006) due to the distribution of nonconforming products.
FDA•MODERATESelenia Dimensions Mammography SystemsHologic recalls Selenia Dimensions mammography systems over loose or broken internal bolts.
2 products
FDA•CRITICALOrganic Peppermint Leaf PowderPure Ground Ingredients recalls Organic Peppermint Leaf Powder over possible Salmonella contamination.
FDA•MODERATEMetoprolol Succinate Extended-Release Tablets 25 mgAscend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.
FDA•MODERATEDexcom G7 CGM iOS AppDexcom recalls G7 CGM iOS App (v2.9.0–2.11.2) over glucose alert delays that may cause missed hypo/hyperglycemic events.
4 products
FDA•MODERATEBuprenorphine Hydrochloride Injection 0.3mg/mLEndo USA recalls Buprenorphine Hydrochloride Injection 0.3mg/mL vials (NDC 42023-179-05) due to particulate matter contamination.
FDA•MODERATEDiowave 250W Laser SystemDiowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.
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•Better Weather Fix ElixirBetter Weather Fix Elixir recalled for undeclared Kratom (Mitragynine) that can cause severe or fatal effects.
FSIS•MODERATECrawford Sausage HeadcheeseCrawford Sausage headcheese may be contaminated with Listeria; produced Jan 20, 2026.
3 products
FDA•CRITICALMG217 Multi-Symptom Treatment CreamMG217 Multi-Symptom Treatment Cream recalled due to Staphylococcus aureus contamination.