FSIS•CRITICAL
Synear Supreme Pork and Crab Soup Dumplings
Synear is recalling frozen pork and crab soup dumplings due to undeclared peanut allergens.
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FDA•MODERATEKirkland Signature Ultra Strength AntacidGuardian Drug is recalling Kirkland Signature Ultra Strength Antacid tablets due to potential metallic particle contamination.
23 products- 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•CRITICALBirch Benders Sweet Potato Pancake and Waffle MixHometown Food Company is recalling Birch Benders Sweet Potato Pancake and Waffle Mix due to an undeclared egg allergen.
FDA•CRITICALRaw Shelled PeanutsWilco Peanut Co. is recalling raw shelled peanuts due to an undeclared tree nut allergen.
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•CRITICALEnoki MushroomsIQ Produce is recalling 150g Enoki Mushrooms due to potential Listeria monocytogenes contamination.
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•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•CRITICALHellas Meze Golden Smoked Whole HerringHellas Meze Golden Smoked Whole Herring is recalled due to potential Clostridium botulinum contamination from un-eviscerated fish.
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•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•CRITICALDraeger Atlan A350 Anesthesia WorkstationDraeger is recalling the Atlan A350 anesthesia workstation (Model 8211500) due to potential piston ventilator failure.
2 products
FDA•CRITICALBoba Time Italian Yogurt PowderSKS Copack is recalling Boba Time Italian Yogurt Powder due to potential Salmonella contamination.
19 products
FDA•CRITICALIvenix Large Volume PumpFresenius Kabi is recalling Ivenix Large Volume Pumps due to potential touchscreen malfunctions caused by internal damage from drops or jarring.
FDA•MODERATENeptune Smart Docking StationStryker is recalling the Neptune Smart Docking Station (120V) due to missing safety testing and a potential electrical shock risk.
- Device RecallFDA•CRITICALIvenix Infusion System LVP Software
Fresenius Kabi is recalling Ivenix Infusion System LVP software due to a potential battery-health reporting error that may cause pump shutdown.
FDA•CRITICALB. Braun Spinal Needle Procedure KitsB. Braun is recalling various spinal needle procedure kits due to quality issues with the included Bupivacaine Hydrochloride injection.
3 products
FDA•CRITICALCheese Sauce MixThe Coffee Connexion is recalling cheese sauce mix products due to potential Salmonella contamination in a dry milk powder ingredient.
4 products
FDA•CRITICALStoltzfus Family Farm Sour Cream and Onion Cheese CurdsStoltzfus Family Dairy is recalling 8-ounce Sour Cream and Onion cheese curds due to potential Salmonella contamination.
FDA•CRITICALSouthern Style Nuts Gourmet Hunter MixJohn B. Sanfilippo & Son is recalling Gourmet Hunter Mix nationwide due to potential Salmonella contamination.
6 products
FDA•CRITICALButter Parsley Bagel CrispsLegacy Bakehouse is recalling Butter Parsley Bagel Crisps due to potential Salmonella contamination from recalled milk powder.
3 products
FDA•CRITICALGuittard 72% Cacao Chocolate with Date Sugar WafersGuittard is recalling 25lb bulk containers of 72% Cacao Chocolate with Date Sugar Wafers due to potential Salmonella contamination.
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•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•CRITICALKayserBett IDA Pediatric Care BedKayserBetten is recalling IDA pediatric care beds due to an entrapment risk if hand controls are not locked while the child is unattended.
FDA•MODERATE...And KimchiOcinet is recalling ...And Kimchi in 126 oz, 63 oz, and 30 oz containers due to an undeclared fish allergen.
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•CRITICALFiery Hot Seasoning (Reduced Salt)JCB Flavors is recalling 25 lb containers of Fiery Hot Seasoning (Reduced Salt) due to potential Salmonella contamination.
10 products
FDA•CRITICALa2 Platinum Premium Infant FormulaThe a2 Milk Company is recalling 31.7oz tins of a2 Platinum Premium infant formula due to potential Cereulide toxin contamination.
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•CRITICALMalazi 100% Pure Sudanese Sesame TahinaNassar Investment Company is recalling Malazi 100% Pure Sudanese Sesame Tahina due to potential Salmonella contamination.
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