FDA•MODERATE
Shimadzu Medical Systems X-Ray and Angiography Generators
Shimadzu is recalling 20+ models of X-ray and angiography systems due to a contactor defect that may keep power active when switched off.
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FDA•CRITICALHeritage Animal Nutrition Medicated FeedHeritage Animal Nutrition is recalling 50 lb bags of medicated feed due to potential rumensin contamination.
FDA•MODERATEFreshKote Lubricant EyedropsHarrow Eye LLC is recalling FreshKote Lubricant Eyedrops (0.33 fl oz) due to lack of assurance of sterility.
FDA•MODERATENegita Cracker ShrimpHadson is recalling Negita Cracker Shrimp 2.8 oz over undeclared FD&C Yellow 6.
FDA•MODERATEPublix Bran FlakesPublix Bran Flakes are being recalled due to the potential presence of plastic foreign material.
FDA•CRITICALBreeder's Edge Foster Care Puppy Milk ReplacerBreeder's Edge is recalling various sizes of Puppy Milk Replacer due to inconsistent vitamin D levels.
2 products- Food RecallFDA•MODERATESilver Moon LP: 48 recalled products
48 Silver Moon LP products recalled over tree nuts, peanuts, milk, eggs, soy, wheat, sulfites, and other hazards.
48 products 
FDA•MODERATECovidien Shiley Tracheostomy TubeCovidien is recalling Shiley Tracheostomy Tubes (REF 6FEN) due to incorrect display box labeling.
FDA•MODERATECovidien EndoStitch Polysorb Single Use Loading UnitCovidien is recalling EndoStitch Polysorb loading units (models 170053 and 170071) due to a compromised sterile barrier.
FDA•MODERATEPhilips Achieva 1.5T MR Elastography SystemPhilips is recalling Achieva 1.5T MRE systems due to a software error that may cause inaccurate stiffness value measurements.
19 products
FDA•MODERATESpecially SELECTED Vanilla Creme BruleeLactalis Canada is recalling Specially SELECTED Vanilla Creme Brulee (3.6 oz) over possible glass contamination.
FDA•MODERATEDexcom G7 CGM iOS AppDexcom is recalling G7 CGM iOS app versions 2.9.0–2.11.2 due to a software defect that may delay glucose alerts and readings.
4 products
FDA•MODERATE52USA Strawberry Popping Boba52USA Strawberry Popping Boba is recalled for containing unapproved food colors including FD&C Yellow 5, Yellow 6, and Red 40.
6 products
FDA•MODERATEPhysio-Control LIFEPAK DefibrillatorsPhysio-Control is recalling various LIFEPAK defibrillators due to missing documentation of required performance inspections.
FDA•MODERATELUCAS Chest Compression SystemJolife AB is recalling LUCAS 2, 3, and 3.1 chest compression systems due to missing service documentation.
2 products
FDA•MODERATESwad Orange Flavored Masala CandyRaja Foods is recalling Swad Orange Flavored Masala Candy due to undeclared FD&C Yellow 6.
2 products
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•MODERATECodman CerebroFlo EVD CatheterIntegra LifeSciences is recalling the CerebroFlo EVD Catheter due to out-of-specification endotoxin results.
FDA•CRITICALArrow Edge Hemodialysis Catheterization Kit Sheath IntroducerArrow is recalling hemodialysis kits containing a defective sheath introducer that may fail to split, risking injury during procedures.
6 products
FDA•MODERATEBard Dynamic Deca Steerable Electrophysiology CatheterStryker is recalling Bard Dynamic Deca Steerable Electrophysiology Catheters due to incomplete sterile packaging seals.
26 products
FDA•MODERATEMedline Eye Tray-LF Convenience KitMedline is recalling Eye Tray-LF kits containing mislabeled Cardinal Health syringes that may lead to incorrect insulin dosing.
FDA•CRITICALMedline Anesthesia TraysMedline is recalling anesthesia trays containing Huons Bupivacaine due to quality concerns, data integrity issues, and reduced efficacy.
7 products
FDA•MODERATEOmega-3-Acid Ethyl Esters Capsules 1 gramMajor Pharmaceuticals is recalling Omega-3-Acid Ethyl Esters Capsules 1 gram (NDC 0904-7495-06) due to failed capsule shell specifications.
FDA•MODERATEThermedx FluidSmart Urology Tube SetStryker is recalling the FluidSmart Urology Tube Set due to the distribution of nonconforming products.
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•CRITICALOrganic Peppermint Leaf PowderPure Ground Ingredients is recalling Organic Peppermint Leaf Powder due to potential Salmonella contamination.
FDA•MODERATEHologic Selenia Dimensions Mammography SystemsHologic is recalling 15+ models of Selenia Dimensions Mammography Systems due to potential internal bolt failure.
2 products- Device RecallFDA•MODERATEMedtronic SynchroMed Flex Infusion Mode A810 App
Medtronic is recalling the A810 software app for SynchroMed pumps due to a display error that can disrupt the programmed infusion schedule.
2 products 
FDA•MODERATESwan-Ganz CathetersBecton, Dickinson and Company is recalling 15+ models of Swan-Ganz Catheters due to a risk of hub leakage or breakage.
3 products
FDA•MODERATEBulk Horchata PowderMarquez Brothers International is recalling Bulk Horchata Powder due to undeclared milk, which poses a risk to those with milk allergies.
3 products
FDA•MODERATEAlendronate Sodium Oral Solution 70 mg/75 mLHikma is recalling Alendronate Sodium Oral Solution 70 mg/75 mL (NDC 0054-0282-59) due to out-of-specification assay results.
FDA•MODERATEBD GasPak EZ Gas Generating Pouch SystemsBecton Dickinson is recalling BD GasPak EZ CO2 and Campy Gas Generating Pouch Systems due to insufficient carbon dioxide production.
2 products
FDA•MODERATEClaravis (isotretinoin capsule, USP) 10 mgTeva is recalling Claravis 10 mg capsules (NDC 0555-1054-56, 0555-1054-86) due to out-of-specification Tretinoin impurity levels.
3 products
FDA•CRITICALKirkland Signature Traditional MadeleinesKirkland Signature Traditional Madeleines are recalled due to undeclared hazelnut and soy lecithin.
FDA•MODERATEDelflex Peritoneal Dialysis SolutionFresenius Medical Care is recalling Delflex Peritoneal Dialysis Solution due to potential bag leaks and a lack of sterility assurance.
2 products
FDA•MODERATEQuickVue Dipstick Strep A TestQuidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
FDA•MODERATELVIS Intraluminal Support DeviceMicroVention recalls LVIS Intraluminal Support Devices (REF 214022-CAS, 214518-CAS, 213517-CAS) due to dimensional nonconformance risking vessel injury or thrombosis.
FDA•MODERATELiquid Blenz Soursop BittersLiquid Blenz Soursop Bitters are recalled due to potential Clostridium botulinum contamination and unauthorized health claims.
13 products
FDA•MODERATEDakota Honey Company Spreadable Spun HoneyDakota Honey Company is recalling Original Spreadable Spun Honey due to potential contamination with stainless steel or plastic foreign objects.
5 products
FDA•MODERATEDePuy Synthes Attune Revision Hinge Femoral ComponentDePuy Synthes is recalling the Attune Revision Hinge Femoral component due to a potential loss of sterility from packaging defects.
9 products
FDA•MODERATEFain's Blackberry Honey SpreadWalker Honey Co. is recalling Fain's Blackberry Honey Spread due to potential stainless steel or plastic particle contamination.
10 products
FDA•MODERATELundberg Family Farms Jasmine White RiceLundberg Family Farms is recalling 32 oz Jasmine White Rice due to potential foreign material contamination.
FDA•MODERATEGrace Medical Stapes ProsthesisGrace Medical is recalling the Titanium/Fluoroplastic Piston Stapes Prosthesis due to incorrect functional length listed on the labeling.
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•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•CRITICALEnoki MushroomsHemu Trading is recalling 150g packages of Enoki Mushrooms due to potential Listeria monocytogenes contamination.
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•CRITICALCook Centimeter Sizing CatheterCook is recalling Centimeter Sizing Catheters due to a risk of marker band breakage, which may cause vessel injury or life-threatening harm.
3 products