FDA•LOW
Primidone Tablets 50 mg
Primidone 50 mg tablets recalled due to possible cross-contamination with Acemetacin.
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FDA•LOWPrimidone 250mg TabletsLannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.
FDA•MODERATEICU Medical Oncology Extension SetICU Medical is recalling Oncology Extension Set REF: CL3960 due to a potential leak that could cause therapy interruption or hazardous exposure.
FDA•WAP Sensual Enhancement CapsulesWAP Sensual Enhancement capsules recalled for undeclared sildenafil, tadalafil, and flibanserin.
FDA•CRITICALKroger Homestyle Cheese and Garlic CroutonsKroger Homestyle Cheese and Garlic Croutons recalled over possible Salmonella from milk powder.
FDA•CRITICALPS Seasoning & Spices: 6 productsPS Seasoning recalls Ellsworth Sour Cream + Onion Seasoning and other seasonings over Salmonella risk.
6 products
FDA•MODERATEOphthavet Ophthalmic SolutionDechra is recalling Ophthavet Ophthalmic Solution for dogs and cats due to a lack of sterility assurance.
FDA•MODERATETangent Single Use Digital CatheterTangent Endoscopy is recalling single-use digital catheters due to potential fractures at the distal shaft tip.
FDA•MODERATESwan-Ganz Catheters (Multiple Models)Becton, Dickinson and Company is recalling multiple variants of its Swan-Ganz pulmonary artery catheters due to a potential risk of valve leakage that may affect the balloon inflation performance.
3 products
FDA•MODERATEStraus Family Creamery: 5 productsStraus Family Creamery recalls Organic Super Premium Ice Cream over possible metal pieces.
5 products
FDA•MODERATEProspector Popcorn Belgian Chocolate Toffee PopcornProspector Popcorn Belgian Chocolate Toffee recalled for undeclared soy (soy lecithin).
2 products
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.
- Device RecallFDA•MODERATEMedtronic SynchroMed Flex Infusion Mode A810 Software
Medtronic is recalling A810 software for SynchroMed pumps due to a display error that may cause incorrect or missed medication delivery.
2 products 
FDA•CRITICALDOXOrubicin Hydrochloride Liposome InjectionSun Pharma recalls DOXOrubicin Liposome Injection 50 mg/25 mL vials due to glass particulate matter.
FDA•CRITICALHellas Meze Golden Smoked Whole HerringTerra Medi is recalling Hellas Meze Golden Smoked Whole Herring due to potential Clostridium botulinum contamination.
FDA•CRITICALEnoki MushroomsIQ Produce is recalling 150g Enoki Mushrooms due to potential Listeria monocytogenes contamination.
FDA•CRITICALEnoki MushroomsHH Fresh Trading is recalling 150g packages of Enoki Mushrooms due to potential Listeria monocytogenes contamination.
FDA•MODERATERaja Foods and Vegetables: 2 Flavored Masala CandiesRaja Foods recalls Swad Orange and Mango Masala Candies due to undeclared FD&C Yellow 6.
2 products
FDA•MODERATECodman CerebroFlo EVD CatheterIntegra LifeSciences is recalling the Codman CerebroFlo EVD Catheter due to out-of-specification endotoxin results.
FDA•CRITICALArrow Edge Hemodialysis Catheterization ProductArrow Edge hemodialysis catheterization product recalled: sheath introducer may not split, risking injury.
6 products
FDA•CRITICALOmnicell i.v.STATION Syringe LabelsOmnicell is recalling sterile syringe label stock for the i.v.STATION device due to a risk of mislabeled IV medication syringes.
FDA•MODERATEBARD Dynamic Deca Steerable CatheterBARD Dynamic Deca Steerable EP catheter recalled due to incomplete seals on sterile product.
26 products
FDA•MODERATEEdwards EVOQUE Tricuspid Delivery SystemEdwards Lifesciences is updating the labeling for the EVOQUE tricuspid delivery system to include a warning about potential functionality issues.
FDA•MODERATECreamy Sesame NoodlesFly By Jing recalls Creamy Sesame Noodles over possible undeclared peanut allergen.
FDA•MODERATEZYMUTEST HIA IgG ELISA KitZYMUTEST HIA IgG ELISA kit lot FD1265 distributed with outdated flyer containing incorrect positive control values.
FDA•MODERATEPhilips Azurion Cable Hose CarrierPhilips is recalling Azurion imaging systems due to potential loosening or breakage of Cable Hose Carrier bolts and plastic parts.
FDA•MODERATEQuickVue Dipstick Strep A TestQuidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
FDA•MODERATEThermedx FluidSmart Urology Tube SetStryker is recalling the FluidSmart Urology Tube Set (REF LL0006) due to the distribution of nonconforming products.
FDA•MODERATESelenia Dimensions Mammography SystemsHologic recalls Selenia Dimensions mammography systems over loose or broken internal bolts.
2 products
FDA•CRITICALOrganic Peppermint Leaf PowderPure Ground Ingredients recalls Organic Peppermint Leaf Powder over possible Salmonella contamination.
FDA•MODERATEMetoprolol Succinate Extended-Release Tablets 25 mgAscend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.
FDA•MODERATEDexcom G7 CGM iOS AppDexcom recalls G7 CGM iOS App (v2.9.0–2.11.2) over glucose alert delays that may cause missed hypo/hyperglycemic events.
4 products
FDA•MODERATEBuprenorphine Hydrochloride Injection 0.3mg/mLEndo USA recalls Buprenorphine Hydrochloride Injection 0.3mg/mL vials (NDC 42023-179-05) due to particulate matter contamination.
FDA•MODERATEDiowave 250W Laser SystemDiowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.
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•Better Weather Fix ElixirBetter Weather Fix Elixir recalled for undeclared Kratom (Mitragynine) that can cause severe or fatal effects.
FSIS•MODERATECrawford Sausage HeadcheeseCrawford Sausage headcheese may be contaminated with Listeria; produced Jan 20, 2026.
3 products
FDA•CRITICALMG217 Multi-Symptom Treatment CreamMG217 Multi-Symptom Treatment Cream recalled due to Staphylococcus aureus contamination.
FDA•Spring & Mulberry Chocolate BarsSpring & Mulberry expands recall of chocolate bars over possible Salmonella contamination.
FDA•MODERATEOasis Tears PF Lubricant Eye DropsOasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.
FDA•MODERATEDakota Honey: 5 CompaniesDakota Honey recalls Spreadable Spun Honey varieties over possible metal/plastic contamination.
5 products
FDA•MODERATERevolution Ascend CTGE HealthCare recalls Revolution Ascend CT over AW Server security vulnerability.
7 products
FDA•CRITICALNamic Angiographic ManifoldMedline recalls Namic Angiographic Manifolds (SKU 64038200) due to particulate in the fluid path.
14 products
FDA•MODERATEAlain Milliat Orange MarmaladeFinesaler recalls Alain Milliat Orange Marmalade 300g jars over possible glass contamination.
FDA•MODERATEDonJoy IceMan Classic CubeDonJoy IceMan Classic Cube recalled due to broken connector interrupting cold therapy.
4 products
FDA•MODERATEOn-X Mitral Heart Valve with Conform-X Sewing RingOn-X is recalling Model ONXMC-25/33 Mitral Heart Valve due to incomplete testing before distribution.
FDA•CRITICALStoltzfus Family Farm Sour Cream and Onion Cheese CurdsStoltzfus Family Farm is recalling 8-ounce Sour Cream and Onion cheese curds due to potential Salmonella contamination.
FDA•CRITICALJonco Industries: 2 productsWhite Cheddar Seasoning recalled over possible Salmonella from milk powder.
2 products
FDA•CRITICALLegacy Bakehouse: 3 Bagel Crisps WisLegacy Bakehouse recalls bagel crisps and pita chips over Salmonella risk from milk powder.
3 products
FDA•CRITICALGeorge J Howe: 6 productsGeorge J Howe recalls sunflower seed products due to undeclared cashew allergen.
6 products