FDA•CRITICAL
D'Dioses Fruit Pops: multiple undeclared allergens
32 D'Dioses Fruit Pops products recalled for undeclared tree nuts or milk.
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FDA•LOWPred Mild Ophthalmic SuspensionAbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.
FDA•MODERATEHydroMARK Breast Biopsy Site MarkerDevicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.
FDA•CRITICALOmnipod 5 PodsInsulet recalls Omnipod 5 Pods over cannula damage causing insulin leaks and under-delivery, risking DKA.
3 products
FDA•CRITICALTNVitamins and Doctor's Pride Moringa CapsulesTotal Nutrition is recalling TNVitamins and Doctor's Pride Moringa capsules due to potential Salmonella contamination.
FDA•MODERATEDexcom G7 Continuous Glucose Monitoring SystemDexcom is recalling stolen G7 sensors that were meant for destruction, posing risks of infection, sensor failure, and inaccurate readings.
FDA•LOWNicotine Transdermal System Patch 14 mgAveva is recalling 14 mg Nicotine Transdermal System Patches due to elevated levels of oxidative-related impurities.
FDA•CRITICALMogo Pure Moringa Oleifera CapsulesMogo Moringa is recalling Pure Moringa Oleifera Capsules due to potential Salmonella Typhimurium contamination.
- Food RecallFSIS•MODERATEOlympia Foods Beef Kofta
Olympia Foods beef kofta served at The Kebab Shop is under a public health alert due to potential E. coli O157:H7 contamination.
FDA•Boner Bears ChocolateJXK Enterprises recalls Boner Bears Chocolate, Lot #BB21125, due to undeclared sildenafil.
- Food RecallFDA•CRITICALRaaw Energy: possible Listeria contamination
37 Raaw Energy products recalled for possible Listeria.
37 products 
FDA•CRITICALSKS Copack: 19 productsSKS Copack recalls Boba Time and Angel drink powders over possible Salmonella contamination.
19 products
FDA•MODERATEToxiBan Charcoal-Kaolin SuspensionLloyd is recalling ToxiBan Charcoal-Kaolin Suspension for domestic animals due to microbial levels exceeding specification limits.
FDA•CRITICALMy Pet Carnivore Coarse Ground Whole GoatMy Pet Carnivore Coarse Ground Whole Goat is recalled due to potential Listeria monocytogenes contamination.
8 products
FDA•CRITICALHoneyville Banana Smoothie MixHoneyville is recalling bulk Banana Smoothie Mix due to potential Salmonella contamination in an ingredient.
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•CRITICALAbiomed Automated Impella ControllerAbiomed is recalling the Automated Impella Controller due to hardware issues that may cause motor control, startup, or power failures.
FDA•CRITICALBolton Medical Thoracic Stent-Graft Delivery SystemBolton Medical Inc. is recalling its Thoracic Stent-Graft delivery system due to a labeling update concerning disconnection of the proximal clasp from the outer control tube, which may prevent release of the stent-graft from the delivery system.
2 products
FDA•CRITICALWhole Foods Market Kitchens Minestrone SoupWhole Foods Market Kitchens Minestrone Soup is recalled due to an undeclared shrimp allergen.
CPSC•ABC Trading Children's ToysABC Trading is recalling toy headbands and electronic pet cages due to a button cell battery ingestion hazard posing a risk of death.
CPSC•WSDZ LED Shot GlassesWSDZ LED shot glasses are recalled due to a battery ingestion hazard that can cause serious injury or death.
CPSC•Bethlehem Lights 10-inch Illuminated Ribbon SpheresBethlehem Lights 10-inch Illuminated Ribbon Spheres are being recalled due to an overheating fire hazard that poses a risk of injury or death.
CPSC•Sierra 125U Youth ATVsSierra 125U youth ATVs are recalled for failing federal safety standards, posing crash, collision, and burn hazards.
CPSC•Orb Funkee Squeeze ToysOrb Funkee squeeze toys are recalled due to the presence of asbestos in their sand filling, posing a serious inhalation risk.
CPSC•PandaEar Portable Hook-On ChairsPandaEar is recalling portable hook-on chairs (models C2102 and BTC-51) due to a fall hazard caused by removable crotch restraints.
CPSC•HomeProGym Resistance BandsHomeProGym is recalling purple 60lb and gray 70lb resistance bands that can detach from the handle, posing an impact injury risk.
FDA•MODERATEFentanyl Citrate Sterile CADD for InjectionIntegraDose is recalling Fentanyl Citrate Sterile CADD for Injection (NDC 71139-6030-1) due to the product being subpotent.
FDA•MODERATENephronex Vitamin B-Complex, Vitamin C & Folic Acid LiquidSafecor Health is recalling Nephronex dietary supplement liquid due to the presence of foreign black particles.
FDA•CRITICALSolina U.S. Holding: 10 productsSolina recalls multiple seasonings over potential Salmonella contamination.
10 products
FDA•CRITICALFontana Flavors: 3 For Further Processing WisFontana Flavors recalls 3 flavor products (white cheddar, cream of mushroom, parmesan) over possible Salmonella.
3 products
FDA•MODERATEPhilips Azurion Image Guided Therapy SystemsPhilips is recalling various Azurion systems due to potential mechanical wear in the Float Tabletop control module affecting table movement.
2 products
FDA•MODERATEPhilips Azurion X-ray Tube Cooling Unit Deaeration HosePhilips recalls Azurion systems: deaeration hose may leak oil, causing cooling failure and low-dose fluoroscopy lockout.
4 products
FDA•MODERATESilastic Foley CathetersC.R. Bard is recalling Silastic Brand Foley Catheters due to surface staining on the devices.
FDA•CRITICALBirch Benders Sweet Potato Pancake and Waffle MixBirch Benders Sweet Potato Pancake and Waffle Mix recalled over undeclared egg.
FDA•MODERATEEstradiol Gel 0.1%ANI Pharmaceuticals is recalling Estradiol Gel 0.1% due to defective packets that may be empty or partially full.
FDA•MODERATECimzia Prefilled SyringesUCB is recalling Cimzia prefilled syringes and starter kits due to a lack of assurance of sterility.
FDA•MODERATEErythromycin Tablets 250 mgZydus recalls Erythromycin 250 mg tablets due to impurity above acceptable limit.
2 products
FDA•MODERATEGlobus Medical OneLIF Integrated FixationGlobus Medical is recalling OneLIF integrated fixation systems because some units may not meet shelf-life specifications, which could affect product performance.
2 products
FDA•MODERATEMedtronic GUNDRY Retrograde CannulaMedtronic recalls GUNDRY Retrograde Cannula over sterile barrier breach risk.
9 products
FDA•MODERATEVitamin B-Complex, Vitamin C & Folic Acid SupplementLlorens Pharmaceuticals is recalling Vitamin B-Complex, Vitamin C & Folic Acid supplement bottles due to foreign black particulate matter.
FDA•MODERATEAllProvide Gently Cooked Chicken Recipe for DogsAllProvide is recalling 16 oz Gently Cooked Chicken Recipe for Dogs due to potential plastic contamination.
FDA•MODERATEGas-X Simethicone 125 mg SoftGelsHaleon is recalling Gas-X Simethicone 125 mg SoftGels (120 count), UPC 3 00674 35041 9, due to incomplete inactive ingredient labeling.
FDA•MODERATEWellnov Supplements: 14 Vitaminally LLC Chandler AzesWellnov recalls liquid multivitamins and supplements over cGMP deviations risking bacterial contamination and C. botulinum.
14 products
FDA•MODERATELiraglutide InjectionLupin is recalling Liraglutide Injection (NDC 70748-346-02 and 70748-346-03) due to white thread-like particulate matter in the cartridge.
FDA•CRITICALMalazi Pure Sudanese Sesame TahinaMalazi 100% Pure Sudanese Sesame Tahina is being recalled due to potential Salmonella contamination.
FDA•MODERATEAtomoxetine HCl CapsulesSafecor Health is recalling Atomoxetine HCl capsules due to a labeling mix-up that may result in patients receiving an incorrect dosage.
FDA•LOWPrimidone Tablets 250 mgAmerican Health Packaging recalls Primidone Tablets 250 mg due to trace Acemetacin contamination.
2 products
FDA•LOWBusulfan InjectionSagent Pharmaceuticals is recalling Busulfan Injection (NDC 25021-241-10) due to failed impurities and degradation specifications.
FDA•LOWPrimidone Tablets 50 mgPrimidone 50 mg tablets recalled due to possible cross-contamination with Acemetacin.
2 products
FDA•LOWPrimidone 250mg TabletsLannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.