FDA•MODERATE
SIGNA Premier MR Scanner Magnet Fittings
GE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.
Filters
Category
Agency
Severity
All Recalls
Back to home ←
FDA•CRITICALMedline NAMIC Angiographic Syringe KitsMedline is recalling NAMIC angiographic syringe kits due to a risk of the rotating adaptor disconnecting during use.
24 products
FDA•MODERATEOlympus SOLTIVE Premium Laser SystemOlympus is recalling the SOLTIVE Premium Laser System due to a power supply defect that may cause inoperability, smoke, or a burning smell.
2 products
FDA•MODERATECardinal Health Monoject Tuberculin Syringe 1 mLCardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.
FDA•MODERATESpacelabs Multi-parameter Command Module Model 91496Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.
FDA•MODERATEMedline Convenience Kits with 10mL SyringesMedline is recalling 10+ convenience kits containing 10mL syringes due to unapproved design changes.
21 products
FDA•Quest Cat Food Chicken RecipeGo Raw is recalling Quest frozen chicken cat food due to potentially low levels of thiamine.
FDA•CRITICALHouse of Flavors Chicago Vanilla Ice CreamHouse of Flavors is recalling 3-gallon tubs of Chicago Vanilla Ice Cream due to an undeclared egg allergen.
FDA•MODERATEPepsin 1:3000 PowderAmerican Laboratories is recalling 50 kg drums of Pepsin 1:3000 Powder due to potential Salmonella contamination.
3 products
FDA•CRITICALButter-Rich PowderBluegrass Ingredients is recalling 50 lb. bags of Butter-Rich Powder due to potential Salmonella contamination.
2 products
FDA•MODERATELevothyroxine Sodium Tablets USP 150 mcgMacleods Pharma recalls Levothyroxine Sodium 150 mcg tablets (NDC 33342-401-44) nationwide due to subpotency.
FDA•MODERATENomida Semaglutide InjectionNew Life Pharma is recalling Nomida Semaglutide Injection due to a lack of assurance of sterility.
4 products
FDA•Boner Bears Chocolate SyrupLockout Supplements is recalling Boner Bears Chocolate syrup due to the presence of undeclared sildenafil.
FDA•MODERATELowes Foods Sour Cream and Onion Potato ChipsLowes Foods sour cream and onion potato chips recalled for inaccurate nutrition labels and undeclared MSG.
FDA•CRITICALDreamland Zaatar Chickpea SaladDreamland is recalling Zaatar Chickpea Salad due to undeclared sesame, soy, and wheat allergens.
2 products
FDA•LOWC2O Coconut Water with PulpC2O Coconut Water with Pulp (17.5 oz) is recalled due to an incorrect ingredient label on the outer box that omits added sugar.
FDA•MODERATESynthes 2.4 Volt Locking Screw TapSynthes is recalling the 2.4 Volt Locking Screw Tap due to a labeling error that resulted in the inclusion of incorrect thread components.
2 products
FDA•MODERATEOlympus PKS Cutting ForcepsOlympus is recalling PKS Cutting Forceps (model 3005PK) because defective welds may cause the device's jaw to break during use.
7 products
FDA•MODERATEMedline Namic GuidewiresMedline is recalling 50+ variants of Namic Guidewires due to the rescission of their 510(k) regulatory clearances.
28 products- Food RecallFDA•MODERATEGreenway Farms Jalapeno Dill Pickle Chips
Greenway Farms is recalling 16 fl oz Jalapeno Dill Pickle Chips due to the lack of a required process authority.
2 products 
FDA•MODERATEKing Harvest HummusKing Harvest is recalling Jalapeno and Roasted Red Pepper Hummus in 10 oz and 17 oz tubs due to potential aluminum piece contamination.
6 products
FDA•MODERATEImu-Tek Colostrum-5 CapsulesImu-Tek is recalling Colostrum-5 dietary supplement capsules due to the product being potentially under-processed.
2 products
FDA•MODERATEAmnesteem Isotretinoin Capsules 40 mgMylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.
FDA•MODERATEStryker CHROMOPHARE Softlit Ring Surgical LightStryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System due to a potential failure of the ceiling cover support assembly.
FDA•MODERATEAtellica CH Enzymatic Hemoglobin A1c (A1c_E)Siemens is recalling Atellica CH A1c_E assays due to a risk of depressed results when processed alongside RCRP on the same analyzer.
FSIS•CRITICALBremer Family Size Italian Style MeatballsRosina is recalling Bremer Family Size Italian Style Meatballs (32 oz, ~64 per package, BEST BY 10/30/26) over possible metal contamination.
FDA•MODERATEGreat Value Fat Free Cottage CheeseSaputo Cheese is recalling Great Value Fat Free Cottage Cheese due to potential under-pasteurization.
5 products
FDA•MODERATEElegance Anterior Cervical PlateClariance-SAS is recalling Elegance Anterior Cervical Plates due to the presence of burrs on the finished product.
2 products
FSIS•CRITICALShera Broadhead Clarias Fish ProductsSobico USA recalls 13,464 lbs of Shera Broadhead Clarias Fish (whole/gutted and steaks) imported without required reinspection; best-before June 23, 2027.
2 products
FDA•MODERATEWillamette Valley Pie Company Blueberry Crumble PieWillamette Valley Pie Company is recalling frozen raw blueberry crumble pies due to potential Listeria monocytogenes contamination.
4 products
FDA•CRITICALMade Fresh Salads Whipped Cream CheeseMade Fresh Salads is recalling 5 lb tubs of Whipped Cream Cheese due to potential Listeria monocytogenes contamination.
14 products
FDA•LOWMei Heong Yuen Tangerine Flavor Roasted PeanutsMei Heong Yuen Tangerine Flavor Roasted Peanuts are recalled due to the presence of cyclamates, an unapproved sweetener.
3 products
FDA•LOWGelatin Capsule Pack for Sodium Iodide I-131 KitInternational Isotopes recalling Gelatin Capsule Packs (NDC 69208-003-15/25/35) for Sodium Iodide I-131 Kit due to failed specifications.
FDA•MODERATETECNIS Eyhance IOL with Simplicity Delivery SystemAMO is recalling TECNIS Eyhance IOLs with Simplicity Delivery Systems because the lens haptic may stick, preventing proper unfolding.
2 products
FDA•MODERATEBioCox 60 Type A Medicated ArticleHuvepharma is recalling BioCox 60 Type A Medicated Article due to failure to meet stability specification requirements.
FDA•CRITICALAll Natural Chicken Chips for DogsElite Treats is recalling All Natural Chicken Chips for Dogs due to potential Salmonella contamination.
FDA•MODERATESunflour Bakery Hamburger BunsSunflour Bakery is recalling 18oz hamburger buns due to undeclared sesame seeds, which pose a risk to those with sesame allergies.
FDA•LOWNilotinib Capsules 150 mgCipla is recalling Nilotinib Capsules 150 mg due to failed stability test results.
2 products
FDA•MODERATEVasocaine SprayHTO Nevada is recalling Vasocaine Spray (Lidocaine HCl 4%, Racepinephrine HCl 0.01%) because stability data does not support the expiry date.
3 products
FDA•MODERATEXTANT MEDICAL Xpress Pedicle Screw SystemXTANT MEDICAL is recalling Xpress Pedicle Screw System 6.5 x 50 mm (X073-6555-DL) due to mislabeling identifying incorrect screw length.
FDA•MODERATEArtoura and CPX 4 Breast Tissue ExpandersMentor Texas is recalling 10+ models of breast tissue expanders due to infusion set needles that may be blunt or break during use.
7 products
FDA•MODERATELeksell Gamma Knife Radiosurgery SystemElekta is recalling Leksell Gamma Knife Perfexion, Icon, and Esprit systems due to potential adapter misalignment during radiation delivery.
FDA•CRITICALAbiomed Impella Purge CassetteAbiomed is recalling Generation 1 purge cassettes due to an increased risk of purge leaks.
2 products
FDA•MODERATEAptima HPV AssayHologic is recalling the Aptima HPV assay (catalog 303585) due to the potential for invalid or false negative results.
FDA•CRITICALHandy Solutions Neck & Shoulders Heating PadHandy Solutions Neck & Shoulders Heating Pad (Model 25607) may overheat and cause burns if folded or placed under the body.
FDA•MODERATECub Pediatric Crib Model FL19HStryker is recalling Cub Pediatric Crib Model FL19H over missing access door warning labels.
FDA•CRITICALBaxter Volara Respiratory Therapy Blue Ventilator Adapter ModuleBaxter is correcting its Volara Respiratory Therapy Blue Ventilator Adapter Module (M07937) due to risks of oxygen desaturation or barotrauma in home care use.
FDA•MODERATEWelch Allyn Spot Vision Screener VS100Welch Allyn is recalling the Spot Vision Screener VS100 due to a screen flickering issue that may pose a seizure risk.
FDA•MODERATESterile Radiology Procedure Kits Model DYNDH1491BMedline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.
FDA•CRITICALYoung Again Pet Food Core Health Dog FoodYoung Again Pet Food Core Health Dog Food recalled for presumptive Salmonella; 10 lb and 25 lb bags affected.