FDA•MODERATE
Fluocinonide 0.05% Cream 15g
Taro recalls Fluocinonide 0.05% Cream 15g tubes due to out-of-spec viscosity.
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FDA•MODERATESemaglutide-Glycine-Cyanocobalamin InjectableNorthwest Compounders is recalling Semaglutide-Glycine-Cyanocobalamin Injectable vials due to lack of assurance of sterility.
FDA•MODERATEInstinct Plus Endoscopic Clipping DeviceWilson-Cook Medical is recalling the Instinct Plus Endoscopic Clipping Device due to a potential for the device to malfunction.
CPSC•Head Ski BootsHead is recalling various ski boot models with fluorescent yellow components due to a fall hazard from potential material deterioration.
CPSC•Besslly Halloween Pumpkin Carving KitsBesslly Halloween Pumpkin Carving Kits (Model CHD-014-2) are recalled due to a serious battery ingestion and chemical burn hazard.
CPSC•Prestige Supernova and Typhoon LightersPrestige is recalling Supernova and Typhoon butane lighters because they lack required child-resistant mechanisms, posing fire and burn risks.
CPSC•Happiness Light LED LightsHappiness Light LED lights are recalled due to a serious battery ingestion hazard that can cause severe internal chemical burns and death.
CPSC•Muscccm Pool Drain CoversMuscccm pool drain covers are recalled due to entrapment and drowning hazards for failing to meet federal safety standards.
CPSC•Member's Mark 7' Pre-Lit Twinkling BuckMember's Mark 7' Pre-Lit Twinkling Buck is recalled due to a burn hazard caused by an overheating resistor.
CPSC•VEEKTOMX Mini Power BanksVEEKTOMX VT103 mini power banks are recalled due to fire and burn hazards from overheating lithium-ion batteries.
CPSC•Shenzhen Shijingjie Male-to-Male Extension CordsShenzhen Shijingjie is recalling male-to-male extension cords (models RY-US-06 and RY_US-1.5) due to electrocution, fire, and CO poisoning risks.
CPSC•ShymeryDirect LED LightsShymeryDirect LED lights are recalled due to a serious battery ingestion hazard and missing safety warnings.
CPSC•Yeeluzan Pool Drain CoversYeeluzan pool drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.
FDA•MODERATEPure Palm Medjool DatesPure Palm Medjool Dates recalled due to mislabeling—coconut-covered bites labeled as regular date bites.
3 products
FDA•MODERATEHydroPeptide Clear Alliance SerumHydroPeptide Clear Alliance Serum recalled due to benzene contamination.
4 products
FDA•MODERATECinacalcet Hydrochloride Tablets 30 mgCipla recalls Cinacalcet HCl 30 mg tablets over N-Nitroso impurity above acceptable limit.
3 products
FDA•MODERATEExchange Select Honey Lemon Cough DropsExchange Select Honey Lemon Cough Drops recalled over quality concerns from FDA inspection.
15 products
FDA•MODERATERemel Yeastone BrothRemel is recalling Yeastone Broth due to the potential for incorrect antimicrobial susceptibility testing results.
FDA•MODERATELinkBio CORE WorkstationLinkBio CORE Workstation (87-9136) may display incorrect Planning Date on Start Case menu.
- Device RecallFDA•MODERATEPhilips AneurysmFlow Software
Philips is recalling AneurysmFlow software because the MAFA ratio provides unreliable prognostic data for aneurysm treatment decisions.
FDA•MODERATEArjo Tenor Mobile Patient LiftArjo Tenor patient lifts (Models KHA1000 US, KHA1010 US) recalled for actuator failure risk causing sudden arm drop.
CPSC•BISSELL Steam Shot OmniReach and Omni Steam CleanersBISSELL is recalling Steam Shot handheld steam cleaners due to a burn hazard from attachments that can detach and expel hot water or steam.
CPSC•Easymake Adult Portable Bed RailsEasymake adult portable bed rails are recalled due to an entrapment and asphyxiation hazard that violates federal safety standards.
CPSC•SCUBAPRO Monorail Weight PocketsSCUBAPRO is recalling Monorail Weight Pockets for BCDs because the D-ring handle can detach, posing a drowning hazard.
CPSC•Maitys Magnetic Drinkware CharmsMaitys magnetic drinkware charms are recalled due to an ingestion hazard from loose magnets that can cause serious injury or death.
CPSC•Iron-Containing Dietary SupplementsThe products lack required child-resistant packaging, posing a risk of serious injury or death from poisoning if swallowed by young children.
CPSC•Wybot Robotic Pool VacuumsWybotics is recalling Osprey 700 Max and S1 robotic pool vacuums due to battery overheating, posing burn and fire hazards.
CPSC•Silks Children's Loungewear SetsSilks children's loungewear sets are recalled for violating federal flammability standards, posing a serious burn risk to children.
CPSC•SNOOZ Breez 2-in-1 Smart Bedroom FansSNOOZ is recalling Breez 2-in-1 Smart Bedroom fans due to an overheating fire hazard caused by power connector corrosion.
FDA•MODERATELanreotide Injection 120 mg/0.5 mLCipla recalls Lanreotide Injection 120 mg/0.5 mL over sterility assurance concerns.
2 products
FDA•MODERATEOmnipaque (iohexol) Injection 350 mg/mLGE Healthcare recalls Omnipaque (iohexol) Injection 350 mg/mL due to particulate matter.
2 products
FDA•MODERATEStryker Sustainability Solution Tourniquet CuffsStryker is recalling tourniquet cuffs that may detach from the bladder, preventing the device from maintaining pressure.
FDA•MODERATECrab CakesConnecticut Crab Co. recalls crab cakes over possible temperature abuse and botulism risk.
FDA•MODERATEImu-Tek Animal Health: 2 productsImu-Tek recalls Colostrum-5 capsules and powder due to under-processing.
2 products
FDA•MODERATEReadyMeals Turkey Bacon & Cheddar Pretzel Duo SandwichF&S Fresh Foods recalls ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwiches over undeclared sesame.
FDA•MODERATEDivided Sunset Multi Collagen PeptidesDivided Sunset Multi Collagen Peptides are recalled for failing to declare egg and fish allergens on the product label.
FDA•MODERATEXanax XR Alprazolam 3 mg TabletsViatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.
FDA•MODERATEIsotretinoin Capsules, USP, 40 mgTeva is recalling 40 mg Isotretinoin Capsules due to potency issues.
2 products
FDA•MODERATEB.R.A.H.M.S PlGF Plus KRYPTORBrahms recalls PlGF Plus KRYPTOR test (REF 859075N) due to QC underestimation risk causing false preeclampsia risk classification.
FDA•MODERATEVancomycin HCl 1.5g in 250mL Sodium Chloride InjectionFagron recalls Vancomycin HCl 1.5g/250mL injection due to sterility concern.
5 products
FDA•MODERATEGeri-Care Artificial Tears Lubricant Eye DropsGeri-Care Artificial Tears Lubricant Eye Drops (0.5 oz, NDC 68788-7266-0) recalled due to lack of sterility assurance.
FDA•MODERATEARTIS pheno and ARTIS Icono Biplane X-ray SystemSiemens is recalling ARTIS pheno and ARTIS Icono X-ray systems (Models 10849000, 11327600, 11328100, 11327700) due to erroneous dose display during patient exams.
FDA•MODERATESpacelabs Multi-parameter Command Module Model 91496Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.
FDA•MODERATELIQUID BLENZ: 13 productsLiquid Blenz recalls 13 herbal tonics and bitters over under-processing, risking botulism.
13 products
FDA•MODERATECook Arterial Pressure Monitoring TrayCook recalls Arterial Pressure Monitoring Trays due to incorrect expiration dates.
19 products
FDA•MODERATESee Luer Cap Set MPC-130Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.
CPSC•Coluans Christmas Light-Up RingsColuans Christmas Light-Up Rings (model SJP-50) are recalled due to a battery ingestion hazard that can cause serious injury or death.
CPSC•Beestech Spiral Children's Tower ToysBeestech spiral children's tower toys (Model Bee-210316-01) are recalled due to a choking hazard from small balls.
CPSC•Granitestone Diamond Pro Blue Sauté PansGranitestone Diamond Pro Blue sauté pans are recalled due to impact and burn hazards from handle screws that can detach when heated.
CPSC•TecFlox Minoxidil Topical SolutionTecFlox minoxidil serum is recalled for failing to meet child-resistant packaging requirements, posing a poisoning risk to children.