FDA•MODERATE
Enalapril Maleate Tablets, USP 20 mg
Rising Pharma is recalling Enalapril Maleate 20 mg tablets (NDC 64980-688-10) due to failed impurities test.
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FDA•MODERATEJoint Nourish Liquid SupplementWellnov Supplements is recalling Joint Nourish liquid supplement due to potential bacterial contamination and C. botulinum concerns.
14 products
FDA•MODERATEOneLIF Interbody CageNovapproach Spine is recalling 60+ variants of OneLIF Interbody Cages due to a risk of inserter attachment failure during surgical procedures.
2 products
FDA•MODERATESilastic Foley CathetersC.R. Bard is recalling Silastic Brand Foley Catheters due to surface staining on the devices.
FDA•MODERATECovidien Mon-a-Therm Esophageal StethoscopeCovidien is recalling Mon-a-Therm Esophageal Stethoscopes with Temperature Sensors because the devices lack FDA clearance.
3 products
FDA•MODERATEArvis Hip & Knee 3.0 Instrument Set ComponentsKico Knee Innovation is recalling Arvis Hip & Knee 3.0 instrument components over potential wear or corrosion on the magnet face.
2 products
FDA•MODERATESharpoint Microsurgical KnifeSurgical Specialties Corporation is recalling mislabeled Sharpoint microsurgical knives that contain 3.0mm blades instead of 2.2mm.
FDA•MODERATEBD PurPrep Sterile SolutionCareFusion is recalling BD PurPrep sterile solution distributed nationwide due to potential contamination and lack of sterility assurance.
2 products
FDA•MODERATEBioFire Joint Infection PanelBioFire is recalling the Joint Infection (JI) Panel due to potential contamination that may cause false positive test results.
FDA•MODERATEExacta Mix Vented Micro-Volume InletBaxter is recalling Exacta Mix Vented Micro-Volume Inlets (Model H938175) due to incorrect filters that may cause clinical complications.
FDA•MODERATESystane Lubricant Eye GelAlcon is recalling Systane Lubricant Eye Gel due to a lack of assurance of sterility.
2 products
FDA•MODERATEWoodstock Organic Shelled EdamameWoodstock Organic Shelled Edamame (10 oz. and 48 oz.) recalled for metal pieces.
FDA•MODERATEDuloxetine Delayed-Release Capsules USP 60mgBreckenridge Pharmaceutical recalls Duloxetine 60mg capsules (NDC 51991-748-90) due to elevated N-nitroso impurity from manufacturing deviations.
FDA•MODERATEFrederik's by Meijer Vanilla Bourbon Trail MixFerris Coffee and Nut Company is recalling 9 oz bags of Vanilla Bourbon Trail Mix due to undeclared wheat and soy allergens.
FDA•MODERATEMedtronic GUNDRY Retrograde CannulaMedtronic is recalling GUNDRY Retrograde Cannula catheters due to a potential sterile barrier breach that may compromise device sterility.
9 products
FDA•MODERATEMAC 5 Resting ECG Analysis SystemsGE is recalling MAC 5 A4 and A5 ECG systems due to a software error that may incorrectly associate clinical data with the wrong patient.
FDA•MODERATEOptase Dry Eye Intense DropsScope Health is recalling Optase Dry Eye Intense Drops (0.33 fl oz, NDC 72972-002-01) due to lack of assurance of sterility.
FDA•MODERATEMy Mochi Strawberry Non-Dairy Frozen DessertThe Mochi Ice Cream Company is recalling Strawberry Non-Dairy Frozen Dessert due to a foreign object found in a retail container.
FDA•MODERATENaproxen Oral Suspension USP 125 mg/5mLAcella Pharmaceuticals is recalling Naproxen Oral Suspension 125 mg/5mL (NDC 42192-619-16) due to lead and lithium contamination above specification.
FDA•MODERATEUncle Giuseppe's Marketplace Milk Chocolate Bridge MixUncle Giuseppe's Marketplace Milk Chocolate Bridge Mix is recalled for undeclared cashews, milk, and soy allergens.
FDA•MODERATEShimadzu Medical Systems X-Ray and Angiography GeneratorsShimadzu is recalling 20+ models of X-ray and angiography systems due to a contactor defect that may keep power active when switched off.
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 potential plastic contamination.
- 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 and MR 7700 MR Elastography SystemsPhilips is recalling MR Elastography systems (models 782130, 781196, 781296) due to a software error that can cause inaccurate stiffness values.
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 performance inspection documentation that may impact device therapy.
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 CandySwad Orange Flavored Masala Candy is being recalled due to the presence of 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•MODERATEBard Dynamic Deca Steerable Electrophysiology CatheterStryker is recalling the Bard Dynamic Deca Steerable Electrophysiology Catheter 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.
FSIS•MODERATEQuality Meat Sky Ranch Marinated Beef and Pork ProductsSky Ranch Meat recalled marinated beef and pork products (1.5-lb containers, Dec 2025–Apr 2026) for undeclared sesame allergen.
4 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•MODERATESelenia Dimensions Mammography SystemsHologic is recalling 15+ models of Selenia Dimensions Mammography Systems due to a risk of loose, missing, or broken internal bolts.
2 products- Device RecallFDA•MODERATEMedtronic SynchroMed Flex Infusion Mode A810 Software
Medtronic is recalling A810 software for SynchroMed pumps due to a display error that can cause incorrect or failed infusion delivery.
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
FSIS•MODERATEWalmart Great Value Dino Shaped Chicken Nuggets — RetractionFSIS retracts alert for Walmart Great Value Dino Nuggets (Feb 10 2027) after confirming no lead contamination.
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