FDA•MODERATE
Omnipaque (iohexol) Injection 350 mg/mL
GE Healthcare recalls Omnipaque (iohexol) Injection 350 mg/mL due to particulate matter.
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FDA•MODERATEStryker Sustainability Solution Tourniquet CuffsStryker is recalling tourniquet cuffs that may detach from the bladder, preventing the device from maintaining pressure.
FDA•CRITICALYoung Again Core Health Dog FoodYoung Again is recalling Core Health dog food due to potential Salmonella contamination.
FDA•CRITICALRaaw Energy Dog Food Chicken MedleyRaaw Energy is recalling Dog Food Chicken Medley (2-lb and 5-lb tubes) due to Listeria, Salmonella, and Campylobacter contamination.
5 products
FDA•CRITICALBlaine Labs: multiple drugsBlaine Labs recalls multiple topical antiseptic/antifungal gels and creams due to Lysinibacillus fusiformis contamination.
9 products
FDA•MODERATECrab CakesConnecticut Crab Co. recalls crab cakes over possible temperature abuse and botulism risk.
FDA•LOWPocas International: 4 Popping Boba RTD TeasPocas recalls Popping Boba RTD teas over packaging integrity issue.
4 products
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•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.
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
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•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.