FDA•MODERATE
Kirkland Signature Ultra Strength Antacid
Guardian Drug is recalling Kirkland Signature Ultra Strength Antacid tablets due to potential metallic particle contamination.
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FDA•Niacin Extended-release TabletsLannett is recalling 1,000 mg Niacin Extended-release Tablets due to failed dissolution specifications.
- Food RecallFSIS•MODERATEOlympia Foods Beef Kofta
Olympia Foods beef kofta served at The Kebab Shop is under a public health alert due to potential E. coli O157:H7 contamination.
FDA•Pasteurized Donor Human MilkUniversity of California Health Milk Bank is recalling donor human milk (lots 001165 and 001198) due to potential plastic particle contamination.
FDA•Xyvona (levorphanol tartrate) 2mg TabletsForte BioPharma is recalling Xyvona (levorphanol tartrate) 2mg tablets due to the FDA's denial of the product's proprietary name.
2 products
FDA•LOWPred Mild Ophthalmic SuspensionAbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.
FDA•LOWLidocaine HCl Injection 2%Eugia US LLC is recalling Lidocaine HCl Injection 2% single-dose vials because the label wrap obscures the barcode, preventing it from scanning.
FDA•MODERATEDeRoyal Covaderm Plus Vascular Access DressingDeRoyal is recalling Covaderm Plus Vascular Access Dressing (Ref 46-406) due to a lack of sterility assurance.
FDA•ToxiBan Charcoal-Kaolin SuspensionLloyd Inc. is recalling ToxiBan Charcoal-Kaolin Suspension due to microbial levels exceeding specification limits.
FDA•LOWNicotine Transdermal System Patch 14 mgAveva is recalling 14 mg Nicotine Transdermal System Patches due to elevated levels of oxidative-related impurities.
FDA•MODERATEDuloxetine DR Capsules 30 mgAsclemed USA is recalling Duloxetine DR Capsules 30 mg due to the presence of a nitrosamine impurity above acceptable intake limits.
FDA•My Pet Carnivore Coarse Ground Whole GoatMy Pet Carnivore Coarse Ground Whole Goat is recalled due to potential Listeria monocytogenes contamination.
8 products
FDA•MODERATEMedtronic Deep Brain Stimulation Pocket Adaptor KitMedtronic is recalling Deep Brain Stimulation Pocket Adaptor Kits (Models 64001 and 64002) due to incorrect Use-By-Dates on the packaging.
2 products
FDA•MODERATEEstradiol Gel 0.1% PacketsANI Pharmaceuticals is recalling Estradiol Gel 0.1% packets due to a defective container issue resulting in empty or partially full packets.
FDA•MODERATEFentanyl Citrate Sterile CADD for InjectionIntegraDose is recalling Fentanyl Citrate Sterile CADD for Injection due to subpotency.
FDA•MODERATEStraus Family Creamery Vanilla Bean Ice CreamStraus Family Creamery is recalling Organic Super Premium Vanilla Bean Ice Cream due to potential metal contamination.
5 products
FDA•MODERATELidocaine HCl Injection USPSpectra Medical Devices is recalling Lidocaine HCl Injection USP single-dose ampules due to a lack of assurance of sterility.
FDA•MODERATEAllProvide Gently Cooked Chicken Recipe for DogsAllProvide is recalling 16 oz Gently Cooked Chicken Recipe for Dogs due to potential plastic contamination.
FDA•MODERATEGas-X Simethicone 125 mg SoftGelsHaleon is recalling Gas-X Simethicone 125 mg SoftGels (120 count), UPC 3 00674 35041 9, due to incomplete inactive ingredient labeling.
FSIS•MODERATEDaisy Brand Headcheese Deli MeatDaisy Brand Headcheese (EST. 21406, USE BY Mar 26 2026) may contain Listeria; do not consume.
FDA•MODERATECimzia Prefilled SyringesUCB is recalling Cimzia prefilled syringes and starter kits due to a lack of assurance of sterility.
FDA•MODERATEFly By Jing Creamy Sesame NoodlesFly By Jing is recalling Creamy Sesame Noodles due to an undeclared peanut allergen.
FDA•Lunds & Byerly's Curry Powder SweetLunds & Byerly's Curry Powder Sweet is recalled due to undeclared sesame seeds.
FDA•MODERATEVitamin B-Complex, Vitamin C & Folic Acid SupplementLlorens Pharmaceuticals is recalling Vitamin B-Complex, Vitamin C & Folic Acid supplement bottles due to foreign black particulate matter.
FDA•Udder Products Yeast BlendNutra Blend is recalling 50 lb bags of Udder Products Yeast Blend due to elevated selenium levels.
FDA•MODERATENeptune Smart Docking StationStryker is recalling the Neptune Smart Docking Station (120V) due to missing safety testing and a potential electrical shock risk.
- Food RecallFDA•Albertsons: multiple undeclared allergens
121 Albertsons store-made items recalled for undeclared tree nuts, fish, or shellfish.
121 products 
FDA•MODERATEMy Wife's SlawMy Wife's Slaw is being recalled due to a lack of required regulatory safety inspections during the manufacturing process.
2 products
FDA•MODERATEAmlodipine and Olmesartan Medoxomil TabletsAscend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, due to failed dissolution specifications.
FSIS•MODERATEGiovanni Rana Rustic Beef Sauce & Burrata RavioliGiovanni Rana ravioli (32-oz, Est. 44870) may contain undeclared shrimp and lobster instead of labeled beef and burrata; shellfish allergen risk.
FDA•LOWBusulfan InjectionSagent Pharmaceuticals is recalling Busulfan Injection (NDC 25021-241-10) due to failed impurities and degradation specifications.
FDA•MODERATEMarket of Choice Vegan Kale Caesar SaladMarket of Choice is recalling Vegan Kale Caesar Salad due to an undeclared sesame allergen in the Za'atar spice.
FDA•MODERATE...And KimchiOcinet is recalling ...And Kimchi in 126 oz, 63 oz, and 30 oz containers due to an undeclared fish allergen.
FDA•LOWPrimidone Tablets 250 mgAmerican Health Packaging is recalling Primidone Tablets 250 mg due to cross-contamination with trace amounts of Acemetacin.
2 products
FDA•Albright's Raw Pet Food Chicken RecipeAlbright's is recalling Raw Pet Food Chicken Recipe for dogs due to potential Salmonella contamination.
FDA•MODERATENephronex Vitamin B-Complex, Vitamin C & Folic Acid LiquidSafecor Health is recalling Nephronex oral liquid supplement due to foreign substance contamination from observed black particles.
FDA•MODERATESecond Nature Keto Crunch Smart MixSecond Nature is recalling Keto Crunch Smart Mix due to undeclared cashews, pistachios, and dried cherries.
FSIS•MODERATEMeat and Poultry Products with Recalled Dairy IngredientsFSIS alerts consumers to meat and poultry products with recalled dairy ingredients potentially contaminated with Salmonella.
FDA•MODERATEOphthavet Ophthalmic SolutionDechra is recalling Ophthavet Ophthalmic Solution for dogs and cats due to a lack of sterility assurance.
FDA•MODERATEAtomoxetine HCl 10mg CapsulesSafecor is recalling Atomoxetine HCl 10mg Capsules (NDC 64380-474-01) because some cartons may contain 25mg capsules due to a labeling error.
FDA•MODERATEPhilips Azurion and Allura Imaging SystemsPhilips is recalling Azurion and Allura imaging systems due to hard disk drive failure that may cause loss of functionality or data.
2 products
FDA•MODERATEHiResolution Bionic Ear SystemAdvanced Bionics is recalling the HiRes Ultra 3D CI HiFocus Mid Scala cochlear implant due to an incorrect shelf-life expiration date.
FDA•MODERATEBD Pyxis MedStation 4000 Fingerprint ScannerCareFusion 303 is recalling the BD Pyxis MedStation 4000 medication cabinet due to a fingerprint scanner overheating burn risk.
8 products- FDA•MODERATEDuloxetine Delayed-Release Capsules 30 mg
Ajanta Pharma is recalling Duloxetine 30 mg capsules due to the presence of an N-nitroso-Duloxetine impurity above recommended safety limits.
3 products 
FDA•MODERATEErythromycin 250 mg TabletsZydus is recalling Erythromycin 250 mg tablets due to the presence of N-Nitroso-Desmethyl-Erythromycin above acceptable intake limits.
2 products
FDA•MODERATEProspector Popcorn Belgian Chocolate ToffeeProspector Popcorn Belgian Chocolate Toffee (UPC 850073852125) recalled for undeclared soy lecithin.
2 products
FDA•MODERATEPhilips Azurion Image-Guided Therapy SystemsPhilips is recalling various Azurion image-guided therapy systems due to potential table movement issues caused by control module wear.
2 products- FDA•MODERATEPhilips Azurion X-Ray Tube Cooling Unit
Philips is recalling X-ray tube cooling units in Azurion systems due to hose degradation and potential oil leakage.
4 products 
FDA•MODERATEOasis Tears PF Lubricant Eye DropsOasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.
FDA•MODERATEMetoprolol Succinate Extended-Release Tablets 25 mgAscend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.