FSIS•MODERATE
Quality Meat Sky Ranch Marinated Beef and Pork Products
Sky Ranch Meat recalled marinated beef and pork products (1.5-lb containers, Dec 2025–Apr 2026) for undeclared sesame allergen.
4 productsFilters
Category
Agency
Severity
All Recalls
Back to home ←
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•MODERATEHologic Selenia Dimensions Mammography SystemsHologic is recalling 15+ models of Selenia Dimensions Mammography Systems due to potential internal bolt failure.
2 products- Device RecallFDA•MODERATEMedtronic SynchroMed Flex Infusion Mode A810 App
Medtronic is recalling the A810 software app for SynchroMed pumps due to a display error that can disrupt the programmed infusion schedule.
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
FDA•LOWCVS Lidocaine Wound GelCVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
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
FDA•MODERATEDelflex Peritoneal Dialysis SolutionFresenius Medical Care is recalling Delflex Peritoneal Dialysis Solution due to potential bag leaks and a lack of sterility assurance.
2 products
FDA•MODERATEQuickVue Dipstick Strep A TestQuidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
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.
FDA•MODERATELiquid Blenz Soursop BittersLiquid Blenz Soursop Bitters are recalled due to potential Clostridium botulinum contamination and unauthorized health claims.
13 products
FDA•MODERATEDakota Honey Company Spreadable Spun HoneyDakota Honey Company is recalling Original Spreadable Spun Honey due to potential contamination with stainless steel or plastic foreign objects.
5 products
FDA•MODERATEDePuy Synthes Attune Revision Hinge Femoral ComponentDePuy Synthes is recalling the Attune Revision Hinge Femoral component due to a potential loss of sterility from packaging defects.
9 products
FDA•MODERATEFain's Blackberry Honey SpreadWalker Honey Co. is recalling Fain's Blackberry Honey Spread due to potential stainless steel or plastic particle contamination.
10 products
FDA•MODERATELundberg Family Farms Jasmine White RiceLundberg Family Farms is recalling 32 oz Jasmine White Rice due to potential foreign material contamination.
FDA•MODERATEGrace Medical Stapes ProsthesisGrace Medical is recalling the Titanium/Fluoroplastic Piston Stapes Prosthesis due to incorrect functional length listed on the labeling.
FDA•MODERATEReadyMeals Turkey Bacon & Cheddar Pretzel Duo SandwichReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich is recalled due to undeclared sesame.
FDA•MODERATESterile Water for Injection USPB. Braun is recalling 3000 mL Sterile Water for Injection USP bags distributed nationwide due to potential sterility and leakage issues.
4 products
FDA•LOWAmprol 25% Medicated ArticleHuvepharma is recalling one bag of Amprol 25% medicated article due to missing lot number and expiration date information.
FDA•MODERATELidocaine HCl Injection 1% 5 mL VialsHuons is recalling Lidocaine HCl injection 1% 5 mL vials due to a lack of assurance of sterility.
9 products
FDA•MODERATEepoc BGEM BUN Test CardSiemens is recalling epoc BGEM BUN Test Cards due to the risk of inaccurate pH and carbon dioxide results that may lead to improper treatment.
FDA•MODERATEPhilips Bridge Prep KitMerit Medical Systems is recalling the Philips Bridge Prep Kit due to potential catheter resistance during use.
4 products
FDA•MODERATEda Vinci X and Xi Surgical System Universal Surgical ManipulatorIntuitive Surgical is recalling USM arm sub-assemblies for da Vinci X and Xi systems due to a risk of internal screw breakage.
2 products
FDA•MODERATEOne Step 10A In Vitro Diagnostic TestDFI is recalling the One Step 10A in vitro diagnostic test because it was distributed without required FDA premarket clearance or approval.
7 products
FDA•MODERATEEpinephrine Injection USP 1 mg/10mLInternational Medication Systems is recalling Epinephrine Injection 1 mg/10mL (NDC 76329-3318-1) due to lack of sterility assurance.
FDA•MODERATESkin Script Blemish Spot TreatmentSkin Script Blemish Spot Treatment recalled over failed stability specifications; UPC 6 10563 13873 9.
FDA•MODERATEPure Palm Medjool DatesPure Palm is recalling Medjool Dates because they are mislabeled and actually contain Coconut Date Bites.
3 products
FDA•MODERATEPhenylephrine Hydrochloride Injectable SolutionWells Pharma is recalling Phenylephrine Hydrochloride Injectable Solution (40mg, 250mL) due to cGMP deviations.
7 products
FDA•MODERATEi-STAT Blood Gas CartridgesAbbott is recalling i-STAT EG7+, EG6+, and G3+ cartridges due to inaccurate blood gas readings that may lead to incorrect clinical decisions.
3 products
FDA•MODERATEBiofire Spotfire Respiratory/Sore Throat PanelBiofire is recalling the Spotfire Respiratory/Sore Throat Panel due to the risk of false negative results and control failures.
FDA•MODERATEZYMUTEST HIA IgG ELISA KitZYMUTEST HIA IgG ELISA kit lot FD1265 distributed with outdated flyer containing incorrect positive control values.
FDA•LOWMagnesium Chloride 6-Hydrate Crystal 500GAvantor is recalling Magnesium Chloride 6-Hydrate Crystal 500G bottles (NDC 10106-2448-1) due to subpotency.
FDA•MODERATEErbe Medical ERBEFLO CleverCap CO2 Tubing/Cap SetsErbe Medical is recalling ERBEFLO CleverCap CO2 tubing and cap sets due to a risk of unintended water flow and potential respiratory injury.
3 products
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•MODERATECoconut Drink 1HEYTEA USA INC is recalling Coconut Drink 1 (1L, UPC 673367992785) due to undeclared milk.
FDA•MODERATEDisposable Mixing Bowls with SpatulaZimmer is recalling Disposable Mixing Bowls with Spatula (Model 00-5049-011-00) due to compromised sterile barrier seals.
FDA•MODERATEBoston Scientific LUX-Dx II Arrhythmia DetectorBoston Scientific is recalling LUX-Dx II arrhythmia detectors due to a software error that prevents proper monitoring and data collection.
2 products
FDA•MODERATEVital Nutrients Aller-C CapsulesBlueroot Health is recalling Aller-C capsules due to undeclared egg, soy, and hazelnut allergens.
FDA•MODERATEPrazosin Hydrochloride Capsules 1mgAppco Pharma is recalling Prazosin Hydrochloride Capsules 1mg due to the presence of N-nitroso-prazosin impurity above acceptable limits.
3 products
FDA•MODERATEMicro-X Rover Mobile X-ray GeneratorMicro-X is recalling the X-ray generator in Rover Mobile X-ray Systems due to a malfunction that can make the device inoperable.
FDA•MODERATEStraumann n!ce PMMA Full-arch RestorationStraumann is recalling n!ce PMMA Full-arch Restoration abutments (Article 010.0304) due to an incorrect screw seat interface.
2 products
FDA•MODERATEEdwards EVOQUE Tricuspid Delivery SystemEdwards Lifesciences is updating labeling for the EVOQUE tricuspid delivery system to include a warning about potential functionality issues.
FDA•MODERATEZarlengo's Double Dark Chocolate GelatoZarlengo's Double Dark Chocolate Gelato is recalled due to an undeclared soy allergen.
5 products
FDA•MODERATEEinstein Bros Bagels Honey Almond ShmearEinstein Bros Bagels is recalling Honey Almond Shmear mislabeled as Plain Cream Cheese due to an undeclared almond allergen.