State
73,833 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
JD & SN Inc. is recalling 4 syringes of Vitamin D3 Oil Injectable Solution due to a lack of assurance of sterility.
Moses Lake Professional Pharmacy is recalling Estradiol 20 mg pellets because the FDA determined there is a lack of assurance of sterility.
The FDA is recalling compounded hydroxocobalamin injectable solution from Moses Lake Professional Pharmacy due to a lack of assurance of sterility.
JD & SN Inc. is recalling 120 mg testosterone pellets because the company cannot ensure the sterile compounded drugs are free from contamination.
JD & SN Inc. is recalling two syringes of Glycopyrrolate Injectable Solution because the company cannot guarantee the product is sterile.
Moses Lake Professional Pharmacy is recalling Methionine/Choline/Inositol injectable solution due to a lack of assurance of sterility.
JD & SN Inc. is recalling 150 vials of Alprostadil/Procaine Injectable Solution due to a lack of assurance of sterility.
Moses Lake Professional Pharmacy is recalling 8 syringes of Papaverine/Phentolamine Injectable Solution because the agency cannot assure the sterility of the compounded drug.
JD & SN Inc. is recalling 70 mg testosterone pellets because the company cannot guarantee the sterility of the compounded drug.
FDA is recalling 100 syringes of Sodium Tetradecyl Sulfate Injectable Solution 3% due to lack of assurance of sterility.
The FDA is recalling Estradiol 12 mg pellets from Moses Lake Professional Pharmacy because the manufacturer cannot ensure the sterile compounded drugs are sterile.
JD & SN Inc. is recalling preservative-free methylcobalamin injectable solution due to a lack of assurance of sterility.
JD & SN Inc. is recalling 2 syringes of Papaverine/Phentolamine/Prostaglandin Injectable Solution because the agency cannot assure the sterility of the compounded drug.
JD & SN Inc. is recalling 155 syringes of TRIMIX injectable solution nationwide due to a lack of assurance of sterility.
JD & SN Inc. is recalling specific syringes of Hydroxyprogesterone Caproate Oil because the FDA cannot ensure the sterile compounded drugs are free from contamination.
FDA is recalling 40 syringes of compounded chorionic gonadotropin from Moses Lake Professional Pharmacy due to lack of assurance of sterility.
FDA is recalling Sermorelin/GHRP-6/GHRP-2 injectable solution from Moses Lake Professional Pharmacy due to lack of assurance of sterility.
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 30 mL syringes of 100% sterile ethyl alcohol for injection due to a lack of assurance of sterility.
JD & SN Inc. is recalling 11 Hydroxocobalamin syringes because the FDA cannot ensure they are sterile. The recall covers units distributed nationwide.
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling Estradiol 30 mg pellets because the company cannot ensure the products are sterile.
JD & SN Inc. is recalling Procaine MDV Injectable Solution due to a lack of assurance of sterility. The recall covers 30mL and 300mL containers distributed nationwide.
JD & SN Inc. is recalling 18-pellet vials of 76 mg Testosterone Pellets because the FDA determined there is a lack of assurance of sterility.
JD & SN Inc. is recalling methylcobalamin/hydroxocobalamin syringes because the company cannot ensure the products are sterile.
American Pure Whey is recalling Body Construct Meal Replacement, Cinnamon Roll flavor, due to undeclared soy and milk allergens.
JD & SN Inc. is recalling 91 vials of compounded testosterone pellets because the FDA cannot assure the sterility of the product.