CPSC•
Ocun Condor HMS Triple Carabiner
Ocun is recalling Condor HMS Triple Carabiners (batches 24003xx–25006xx) due to gate malfunction risk causing falls.
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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•LOWAmprol 25% Medicated ArticleHuvepharma is recalling one bag of Amprol 25% medicated article due to missing lot number and expiration date information.
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
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•MODERATESkin Script Blemish Spot TreatmentSkin Script Blemish Spot Treatment recalled over failed stability specifications; UPC 6 10563 13873 9.
FDA•MODERATEPure Palm Medjool DatesPure Palm is recalling Medjool Dates because they are mislabeled and actually contain Coconut Date Bites.
3 products
FDA•MODERATEPhenylephrine Hydrochloride Injectable SolutionWells Pharma is recalling Phenylephrine Hydrochloride Injectable Solution (40mg, 250mL) due to cGMP deviations.
7 products
FDA•MODERATEi-STAT Blood Gas CartridgesAbbott is recalling i-STAT EG7+, EG6+, and G3+ cartridges due to inaccurate blood gas readings that may lead to incorrect clinical decisions.
3 products
FDA•MODERATEBiofire Spotfire Respiratory/Sore Throat PanelBiofire is recalling the Spotfire Respiratory/Sore Throat Panel due to the risk of false negative results and control failures.
FDA•MODERATEZYMUTEST HIA IgG ELISA KitZYMUTEST HIA IgG ELISA kit lot FD1265 distributed with outdated flyer containing incorrect positive control values.
FDA•LOWMagnesium Chloride 6-Hydrate Crystal 500GAvantor is recalling Magnesium Chloride 6-Hydrate Crystal 500G bottles (NDC 10106-2448-1) due to subpotency.
FDA•MODERATEErbe Medical ERBEFLO CleverCap CO2 Tubing/Cap SetsErbe Medical is recalling ERBEFLO CleverCap CO2 tubing and cap sets due to a risk of unintended water flow and potential respiratory injury.
3 products
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•MODERATECoconut Drink 1HEYTEA USA INC is recalling Coconut Drink 1 (1L, UPC 673367992785) due to undeclared milk.
FDA•MODERATEDisposable Mixing Bowls with SpatulaZimmer is recalling Disposable Mixing Bowls with Spatula (Model 00-5049-011-00) due to compromised sterile barrier seals.
FDA•MODERATEBoston Scientific LUX-Dx II Arrhythmia DetectorBoston Scientific is recalling LUX-Dx II arrhythmia detectors due to a software error that prevents proper monitoring and data collection.
2 products
FDA•MODERATEVital Nutrients Aller-C CapsulesBlueroot Health is recalling Aller-C capsules due to undeclared egg, soy, and hazelnut allergens.
FDA•MODERATEPrazosin Hydrochloride Capsules 1mgAppco Pharma is recalling Prazosin Hydrochloride Capsules 1mg due to the presence of N-nitroso-prazosin impurity above acceptable limits.
3 products
FDA•MODERATEMicro-X Rover Mobile X-ray GeneratorMicro-X is recalling the X-ray generator in Rover Mobile X-ray Systems due to a malfunction that can make the device inoperable.
FDA•MODERATEStraumann n!ce PMMA Full-arch RestorationStraumann is recalling n!ce PMMA Full-arch Restoration abutments (Article 010.0304) due to an incorrect screw seat interface.
2 products
FDA•MODERATEEdwards EVOQUE Tricuspid Delivery SystemEdwards Lifesciences is updating labeling for the EVOQUE tricuspid delivery system to include a warning about potential functionality issues.
CPSC•4our Kiddies Tip Restraint Kits4our Kiddies plastic tip restraint kits can break or degrade, posing tip-over hazards to children and elderly consumers.
CPSC•DuraTrac Stainless Steel Gas ConnectorsDuraTrac stainless steel gas connectors (May–Nov 2025, CSA 259973, codes 24D/25A/25B/25C) recalled for fire hazard from gas leaks.
CPSC•AirClub Convertible BassinetsAirClub convertible bassinets (Model QX-831) recalled for fall hazard due to unsafe bed-attachment mechanism.
CPSC•MPINOI Adult Portable Bed RailsMPINOI adult portable bed rails (15"W × 26"H) recalled for entrapment and asphyxiation risk; sold on Amazon Dec 2025–Feb 2026.
CPSC•Nexgrill Metal Wire Bristle Grill BrushesNexgrill is recalling 10.2M metal wire grill brushes (models 530-0024, 530-0034, 530-0039, 530-0041, 530-0042) sold at Home Depot over detachable bristles posing ingestion and internal injury risk.
CPSC•GLMZZ Fidget Magnet Ball Toy SetsGLMZZ Fidget Magnet Ball Toy Sets with high-powered magnets pose serious ingestion hazard to children; sold on Amazon Feb–Oct 2025.
CPSC•FUNTOK 24V 2-Seater Ride-On TruckFUNTOK 24V 2-Seater Ride-On Truck (model DLS-K03) recalled for circuit board fire and burn hazards.
CPSC•Sunnyyes LED Mini LightsSunnyyes LED mini lights recalled for easily accessible lithium coin batteries posing serious ingestion hazard to children.
CPSC•CCCEI Brand Power StripsCCCEI power strips (6ft, 10ft, 15ft cords) lack overcurrent protection and pose fire risk if overloaded.
CPSC•Petzl Nomic and Ergonomic Ice Climbing AxesPetzl is recalling Nomic and Ergonomic ice climbing axes due to shaft breakage at the handle during use, posing a fall hazard.
CPSC•DIY Sauna Heater KitDIY Cold Plunge is recalling DIY Sauna Heater Kits due to overheating electrical conductors that pose a fire hazard and risk of serious injury or death.
CPSC•Vive Health Adult Portable Bed RailsVive Health is recalling 122,000 adult bed rails (models LVA2009SLV, LVA2097SLV, LVA1024) over entrapment and asphyxiation risk; two deaths reported.
FDA•MODERATEZarlengo's Double Dark Chocolate GelatoZarlengo's Double Dark Chocolate Gelato is recalled due to an undeclared soy allergen.
5 products
FDA•MODERATEEinstein Bros Bagels Honey Almond ShmearEinstein Bros Bagels is recalling Honey Almond Shmear mislabeled as Plain Cream Cheese due to an undeclared almond allergen.
FDA•MODERATEPantoprazole Sodium Delayed-Release Tablets 40 mgCamber Pharmaceuticals is recalling Pantoprazole Sodium 40 mg tablets (NDC 31722-713-10) due to discoloration.
FDA•MODERATEImmy Myco DDR Trident Neutralization Buffer BImmuno-Mycologics is recalling Myco DDR Trident Neutralization Buffer B due to potential contamination.
FDA•MODERATESpacelabs Ultraview SL Command ModuleSpacelabs is recalling the SL Command Module due to a manufacturing issue with the electrical leakage tester.
2 products
FDA•MODERATEGE Revolution CT SystemsGE is recalling Revolution CT systems due to a security vulnerability in the AW Server software used with the CT Smart Subscription feature.
7 products