FDA•MODERATE
Midodrine Hydrochloride Tablets, USP 5 mg
Major Pharmaceuticals is recalling Midodrine Hydrochloride Tablets 5 mg (NDC 0904-6818-06) due to inadequately sealed blister packaging.
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FDA•MODERATESee Luer Cap Set MPC-130Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.
FDA•MODERATEMedline Airway Exam Kit Biopsy ValveMedline is recalling Airway Exam Kits containing Olympus biopsy valves due to a risk of rubber fragments detaching during use.
8 products
FDA•CRITICALAbiomed Automated Impella ControllerAbiomed is recalling Automated Impella Controllers due to a potential delay in the "Purge System Blocked" alarm.
2 products
FDA•MODERATEConvatec EsteemBody Drainable PouchConvaTec is recalling the EsteemBody Drainable Pouch due to a manufacturing issue that may cause the pouch to leak.
3 products
FDA•MODERATEKLG Kesar MukhwasGanesha Enterprises is recalling KLG Kesar Mukhwas (200 gm) for undeclared food colorings and unapproved dye.
FDA•CRITICALRosabella Moringa Dietary Supplement CapsulesAmbrosia Brands is recalling Rosabella Moringa dietary supplement capsules due to potential Salmonella contamination.
FDA•MODERATESemaglutide Compounding IngredientHarbin Jixianglong Biotech is recalling Semaglutide for compounding use due to CGMP deviations and lack of required validation testing.
2 products
FDA•MODERATEAmantadine HCl Capsules 100 mgAvKARE is recalling Amantadine HCl Capsules 100 mg (NDC 50268-069-15) nationwide due to failed dissolution specifications.
FDA•MODERATEMedtronic MiniMed Infusion PumpsMedtronic is recalling various MiniMed infusion pumps due to risks of insulin over- or under-delivery that can cause severe health complications.
14 products
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical is recalling 25+ models of CentrosFLO Hemodialysis Catheters due to a sheath design defect that may cause serious injury.
5 products
FDA•MODERATEMedline ENFit G-Tube Connector KitsMedline is recalling G-Tube care and discharge kits due to connector defects that may cause leakage and fluid loss.
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•CRITICALQuest Cat Food Chicken Freeze Dried NuggetsSteve's Real Food recalling Quest Cat Food Chicken Freeze Dried Nuggets (10 oz) over inadequate thiamine levels.
2 products
CPSC•CheerKid Baby Bath SeatsCheerKid baby bath seats (Model BH-222) recalled for tipping risk and drowning hazard.
CPSC•Watkins Highlife Collection Spa Hydromassage Rotary JetsWatkins is recalling Hydromassage rotary jets in Highlife Collection spas (2023–2025) due to entanglement and drowning hazards from suction force.
CPSC•Beloems Adult Portable Bed Rails Model BL-BR201Beloems bed rails (model BL-BR201) recalled for entrapment, asphyxiation, and fall hazards.
CPSC•Fortemotus Direct Adult Portable Bed RailsFortemotus Direct recalls model USFTMTJAS008 adult bed rails (30"×30") sold Aug–Oct 2025 over entrapment, asphyxiation, and fall hazards.
CPSC•SOOWERY 6-Drawer DresserSOOWERY 6-Drawer Dressers (47.2" × 11.8" × 33.3") sold on Amazon pose tip-over and entrapment hazards without wall anchoring.
CPSC•Cositas Colombianas Magnetic Board GamesCositas Colombianas magnetic board games recalled due to loose magnets posing serious ingestion hazard to children.
CPSC•LShome Photoelectric Smoke Detector Fire AlarmsLShome smoke detector alarms (Model XG-7D04-KZ9Z) may fail to sound during fire due to sensing threshold defect.
FDA•CRITICALIQF BlueberriesOregon Potato Company is recalling IQF blueberries in 30 lb. cases and 1400 lb. totes due to potential Listeria monocytogenes contamination.
FDA•LOWEptifibatide Injection 75 mg/100 mLSlate Run Pharmaceuticals recalls Eptifibatide Injection 75 mg/100 mL vials (NDC 70436-027-80, 70436-163-80) due to incorrect dosing-route labeling.
FDA•CRITICALErbe Flexible CryoprobeErbe is recalling Flexible Cryoprobes (REF 20402-401) due to a risk of the probes rupturing or bursting during use.
4 products
FDA•MODERATEOlympus Endoscope Suction ValvesOlympus is recalling MAJ-1443 and MAJ-1444 endoscope suction valves due to compatibility issues with specific automated reprocessors.
4 products
FDA•MODERATEXZL Jelly SnacksXZL Jelly Snacks are recalled due to undeclared FD&C Yellow #5, Yellow #6, and Red #40 food dyes.
FSIS•CRITICALCS Beef Packers Ground Beef ProductsCS Beef Packers recalls 22,912 lbs of ground beef (case codes 18601, 19583, 19563) over E. coli O145 contamination; do not serve.
3 products
FDA•CRITICALJunebar Chocolate Cherry Snack BarJunebar Chocolate Cherry Snack Bar is recalled due to undeclared milk and soy allergens.
4 products
FDA•CRITICALWhite Vein Advanced Alkaloids Chewable TabletsShaman Botanicals is recalling White Vein Advanced Alkaloids Chewable Tablets because the active ingredient exceeds the labeled amount.
2 products
FDA•MODERATEBurlington Medical Wrap ApronsBurlington Medical is recalling Wrap Aprons due to potential attenuation degradation that may reduce the product's lifespan.
13 products
FDA•MODERATEEmbrace Shoulder Instrument Drill TowerWaldemar Link is recalling the Embrace Shoulder Instrument Drill Tower due to incorrect article numbers in the surgical technique documentation.
2 products
FDA•MODERATEBD Alaris System with Guardrails Suite MXBD Alaris System labeling lacks required TLS version specification for secure Wi-Fi communication with Point-of-Care Units.
FDA•MODERATEWellsley Farms Farm-Raised Atlantic SalmonWellsley Farms Farm-Raised Atlantic Salmon (32 oz) recalled for Listeria monocytogenes contamination.
FDA•MODERATEVergani 1944 Milano Pandoro Classico Gluten FreeItalianway Import is recalling Vergani 1944 Milano Pandoro Classico Gluten Free due to potential Teflon fragment contamination.
FDA•MODERATEAdbry (tralokinumab-ldrm) Injection 300 mg/2mLLEO Pharma is recalling Adbry injection autoinjectors (NDC 50222-350-91, 50222-350-02) due to wool fiber contamination affecting sterility.
FDA•MODERATEOrtho Dev. Trimax Lantern Knee Drill PlateOrtho Dev. Trimax Pegged Drill Plates for the Lantern Knee System are recalled due to a manufacturing error causing excessive bone cuts.
2 products
FDA•MODERATEArtegraft Vascular GraftLeMaitre Vascular is recalling Artegraft Vascular Grafts due to a labeling mix-up that resulted in incorrect lot information on packaging.
FDA•MODERATEPuracol and Puracol Plus Collagen Wound DressingsMedline is recalling Puracol and Puracol Plus wound dressings due to elevated endotoxin levels that may cause severe inflammatory responses.
FDA•MODERATEEndoVive Safety PEG KitBoston Scientific is recalling EndoVive Safety PEG Kits due to potentially compromised sterile packaging on included ChloraPrep swabsticks.
CPSC•Aroeve Air Purifier Model MK04Aroeve air purifier model MK04 (serial "BN") recalled for fire and burn hazard due to overheating.
FDA•MODERATEFrozen Cooked Medium ShrimpH & N Group is recalling 1 lb bags of frozen cooked medium shrimp due to potential Cesium-137 contamination.
FDA•MODERATEHortex Spring Vegetable MixHortex Spring vegetable mix is being recalled due to potential contamination with glass.
FDA•MODERATECetrorelix Acetate for Injection Kit 0.25 mgMeitheal Pharmaceuticals recalls Cetrorelix Acetate injection kits (NDC 71288-558-90) due to missing or duplicated needles.
FDA•MODERATERefleXion X1 Radiotherapy System Model RXM1000RefleXion X1 Radiotherapy System Model RXM1000 recalled for software defect causing incorrect radiation dose delivery.
FDA•MODERATEID NOW Influenza A & B 2 Test KitAbbott is recalling ID NOW Influenza A & B 2 test kits (Model 427-000) due to an increased rate of invalid test results.
FDA•MODERATEsmart & simple Turmeric PelletsSmartPak Equine is recalling smart & simple Turmeric Pellets due to elevated aflatoxin levels.
FDA•CRITICALLobster and Crab RavioliPerfect Pasta is recalling Lobster and Crab Ravioli due to undeclared shrimp, crab, lobster, pollock, whiting, and soy allergens.
FDA•MODERATEValley Springs 100% Natural Bottled WaterValley Springs is recalling 100% Natural Bottled Water (1 Gal) due to insanitary bottling conditions.
4 products
FDA•MODERATEArtelon FlexBand Dynamic MatrixInternational Life Sciences is recalling the Artelon FlexBand Dynamic Matrix due to failure to meet bacterial endotoxin testing requirements.
3 products
FDA•CRITICALTRUE METRIX Blood Glucose Meter Owner's BookletsTrividia Health is recalling TRUE METRIX meter manuals due to inadequate instructions for addressing the E-5 error code.
7 products