CPSC•
SEGMART Mini Round Toddler Trampolines
SEGMART is recalling 55-inch toddler trampolines with accessory kits due to a strangulation hazard from the hammock, punching bag, and rings.
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CPSC•Sweetcrispy Electric Pressure WashersSweetcrispy is recalling model XCJ-K01 electric pressure washers due to a serious risk of shock and electrocution from a missing GFCI.
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•MODERATEMedline CENTURION Circumcision KitMedline is recalling CENTURION Circumcision Kit (CIT7050F) due to one lot distributed without sterilization.
FDA•MODERATEPhilips Spectral CT on RailsPhilips Spectral CT on Rails (Model 728334) requires a software update to address gantry positioning, message display, and menu option issues.
FDA•MODERATEEpinephrine Injection USP 1 mg/10mLInternational Medication Systems is recalling Epinephrine Injection 1 mg/10mL (NDC 76329-3318-1) due to lack of sterility assurance.
FDA•MODERATECytal Wound Matrix 2-Layer 5x5 cmCytal Wound Matrix 2-Layer 5x5 cm recalled over out-of-specification endotoxin results.
5 products
FDA•MODERATEReact Health PHOENIX 5L Oxygen ConcentratorReact Health PHOENIX 5L Oxygen Concentrator recalled due to devices not meeting quality specifications.
FDA•CRITICALB. Braun STREAMLINE Bloodline SetB. Braun recalls STREAMLINE bloodline sets for Dialog DR over arterial line air bubble risk.
6 products
FDA•MODERATEElegance Anterior Cervical PlatesClariance-SAS is recalling Elegance Anterior Cervical Plates due to the presence of burrs on the finished product.
2 products
FDA•MODERATEHuons: Multiple Rx Only InjectionsHuons recalls injectable lidocaine, bupivacaine, and saline due to sterility concerns.
9 products
FDA•LOWIsland Kinetics: multiple gelsIsland Kinetics recalls hydrocortisone 1% gels (Remedy Gel, Skin Rehab, Essential Calming) due to subpotency.
3 products
FDA•MODERATEAlbuterol Sulfate Inhalation Solution 0.5%Nephron SC recalling Albuterol Sulfate Inhalation Solution (NDC 69374-330-05) due to illegible labeling.
FDA•MODERATEFluocinonide 0.05% Cream 15gTaro recalls Fluocinonide 0.05% Cream 15g tubes due to out-of-spec viscosity.
3 products
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•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•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•CRITICALBlaine Labs: multiple drugsBlaine Labs recalls multiple topical antiseptic/antifungal gels and creams due to Lysinibacillus fusiformis contamination.
9 products
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•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•CRITICALMedline Convenience Kits with Namic RA SyringesMedline recalls convenience kits with Namic RA syringes over risk of loose connection or disconnection during use.
25 products
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.