FDA•MODERATE
Spacelabs Multi-parameter Command Module Model 91496
Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.
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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.
FDA•CRITICALWawa Beverage: 4 productsWawa recalls 16 oz Iced Tea Lemon, Diet Iced Tea Lemon, Diet Lemonade, and Fruit Punch over undeclared milk allergen.
4 products- Food RecallFDA•Karns Foods Mini Dark Chocolate Raspberry Cups
Karns Foods recalls 8-oz Mini Dark Chocolate Raspberry Cups due to undeclared peanuts.
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.
CPSC•HTRC and Haisito T400 Battery ChargersHTRC and Haisito T400 battery chargers are recalled due to a fire hazard that can cause serious injury or death.
CPSC•Elenker Portable Bed RailsElenker portable bed rails are recalled due to a serious entrapment and asphyxiation hazard that violates federal safety standards.
CPSC•Ocun Condor HMS Triple CarabinersOcun is recalling Condor HMS Triple Carabiners because the gate may fail to close automatically, posing a serious fall hazard.
CPSC•Universal Broadmoor Canopy Bed FramesSamson International is recalling Universal Broadmoor canopy bed frames due to a collapse hazard that poses a risk of impact and injury.
CPSC•Member's Mark Children's Pajama SetsMember's Mark children's pajama sets are recalled for violating federal flammability standards, posing a risk of burn injuries.
CPSC•Tuymec Minoxidil Hair Growth KitsTuymec Minoxidil Hair Growth Kits are recalled due to a lack of child-resistant packaging, posing a poisoning risk to young children.
CPSC•Gavoyeat Halloween Light-Up RingsGavoyeat Halloween Light-Up Rings (model 43398-68657) are recalled due to a battery ingestion hazard that can cause serious injury or death.
CPSC•Sangohe Adult Portable Bed RailsSangohe is recalling models 504E and 504Q adult portable bed rails due to serious entrapment and asphyxiation hazards.
FDA•MODERATEZarlengo Italian Ice: 5 White Round Food And Freezer GradesZarlengo's recalls Chocolate Gelato (multiple sizes) over undeclared soy allergen.
5 products
FDA•MODERATEFresenius Kabi: Multiple Sale NDC Number InjectionsFresenius Kabi recalls 14 lots of Sodium Chloride and Dextrose Injections due to sterility concerns.
14 products
FDA•MODERATEXTANT MEDICAL Xpress Pedicle Screw SystemXTANT MEDICAL is recalling Xpress Pedicle Screw System 6.5 x 50 mm (X073-6555-DL) due to mislabeling identifying incorrect screw length.
FDA•MODERATETornier HRS Max Tuberosity Body and Trial PartsTornier is recalling shoulder system components incorrectly labeled as HRS Max parts, as they are incompatible with the HRS Max system.
FDA•MODERATESmart & Simple Turmeric PelletsSmartPak Equine is recalling Smart & Simple Turmeric Pellets for horses due to elevated aflatoxin levels.
FDA•CRITICALRaw Farm: 5 productsRaw Farm recalls raw cheddar cheeses over possible E. coli O157:H7 outbreak.
5 products
FDA•MODERATECoconut Drink 1HEYTEA USA INC is recalling Coconut Drink 1 (1L, UPC 673367992785) due to undeclared milk.
FDA•MODERATEMedline Anterior Hip Pack Biopsy ValveMedline is recalling Anterior Hip Packs containing Olympus biopsy valves over risk of rubber fragment detachment.
8 products
FDA•MODERATESIGNA Premier MR Scanner Magnet FittingsGE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.
FDA•MODERATEMedtronic MiniMed Insulin PumpsMedtronic MiniMed recalls all Paradigm, 600, and BLE 700 series insulin pumps over insulin delivery errors that can cause severe hypoglycemia or ketoacidosis.
14 products
FDA•MODERATEBurlington Medical Wrap ApronsBurlington Medical wrap aprons may lose shielding effectiveness over time.
13 products
FDA•MODERATEOXOID Microbact 12L Listeria Identification KitOxoid is recalling Microbact 12L Listeria Kit (MB1128A, Lot 4494873) due to risk of incorrect organism identification from ambiguous color reactions.
- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo O2 Ventilator
Philips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 products 
FDA•MODERATECardinal Health Monoject Tuberculin Syringe 1 mLCardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.
FDA•CRITICALDouble Down Deer FeedProducers Cooperative Association is recalling Double Down deer feed products due to elevated aflatoxin levels.
2 products
FDA•MODERATEPurina Nature's Match Sow & Pig Complete FeedPurina is recalling 50 lb bags of Nature's Match Sow & Pig Complete Feed (UPC 804273051451) due to elevated Deoxynivalenol levels.
FDA•LOWTops Markets: 2 Peeled GarlicsPeeled Garlic recalled over Clostridium botulinum risk from temperature abuse.
2 products
FDA•MODERATELucerne 2% Cottage Cheese 24 ozLucerne 2% Cottage Cheese 24 oz recalled over possible metal fragments.
FDA•LOWSuper World Trading: 3 Heshan Mei Heong Yuen Food Pte NiesMei Heong Yuen roasted peanuts recalled over banned cyclamate sweetener.
3 products
FDA•MODERATEMeclizine Hydrochloride Tablets 12.5 mgAmerican Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.
FDA•MODERATEeTRAX Needle System Starter Kit 12GCivco recalls eTRAX Needle System Starter Kit 12G (Part 667-149) due to sensor programming error causing incorrect needle tip position.
8 products
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical recalls CentrosFLO Hemodialysis Catheters over sheath introducer defect that may cause hemorrhage and other serious complications.
5 products
FDA•CRITICALBaxter Volara Ventilator Adapter ModuleBaxter is issuing a correction for the Volara Respiratory Therapy system adapter module to prevent oxygen desaturation and lung injury.
FDA•Kian Pee Wan Dietary Supplement CapsulesKian Pee Wan capsules recalled for undeclared dexamethasone and cyproheptadine.
FDA•CRITICALSpray Dried Dairy PowderLone Star Dairy Products is recalling Spray Dried Dairy Powder (25 kg bags, 1 metric ton totes) due to Salmonella contamination.
FDA•MODERATEPrazosin Hydrochloride Capsules 1mgAppco Pharma recalls Prazosin HCl 1mg capsules over nitrosamine impurity (NNP) above acceptable limits.
3 products
FDA•MODERATEK.C. Pharmaceuticals: Multiple Eye DropsK.C. Pharmaceuticals recalls multiple brands of sterile eye drops over sterility concerns.
15 products
FDA•CRITICALAbiomed Impella Purge CassetteAbiomed is recalling Generation 1 purge cassettes due to an increased risk of purge leaks.
2 products
FDA•MODERATEBromfenac Ophthalmic Solution 0.07%Alembic Pharmaceuticals is recalling Bromfenac Ophthalmic Solution 0.07% (NDC 62332-583-03) due to failed impurities and degradation specifications.
FDA•MODERATEJFE FRANCHISING: 7 productsJFE recalls Dumpling Party Trays and Loaded Dumpling Vegetable products over possible glass contamination.
7 products
FDA•MODERATETramadol Hydrochloride Tablets 50 mgAmneal is recalling 500-count bottles of Tramadol Hydrochloride 50 mg tablets due to an impurity found during stability testing.
FDA•MODERATECurosurf (poractant alfa) 240 mg Intratracheal SuspensionChiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.