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.
Moses Lake Professional Pharmacy is recalling Estradiol 25 mg pellets because the agency cannot assure the sterility of the compounded drug.
American Pure Whey is recalling Build Your Own Body Protein Powder due to undeclared soy and milk allergens.
Moses Lake Professional Pharmacy is recalling 22 vials of a compounded injectable solution due to a lack of assurance of sterility.
The FDA is recalling Estradiol Pellets, 6 mg, compounded by JD & SN Inc. because the agency cannot assure the sterility of the product.
JD & SN Inc. is recalling 6 syringes of Methylcobalamin Injectable Solution due to a lack of assurance of sterility. The recall covers all sterile human compounded drugs within their expiry.
JD & SN Inc. is recalling 130 mg testosterone pellets because the company cannot ensure they are sterile.
Moses Lake Professional Pharmacy is recalling 41 syringes of Sermorelin/GHRP-6/GHRP-2 injectable solution because the FDA cannot assure the sterility of the compounded drug.
FDA is recalling 42 syringes of compounded chorionic gonadotropin from Moses Lake Professional Pharmacy due to lack of assurance of sterility.
JD & SN Inc. is recalling compounded progesterone pellets because the agency cannot ensure they are sterile. Consumers should stop using the product and contact their healthcare provider.
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling Vitamin B-Complex Injectable Solution due to a lack of assurance of sterility.
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling six syringes of Folic Acid Injectable Solution because the sterility of the compounded drug cannot be assured.
JD & SN Inc. is recalling specific syringes of Methylcobalamin injectable solution because the agency could not ensure the product remained sterile.
FDA is recalling 2 syringes of injectable glutathione from Moses Lake Professional Pharmacy because the sterility of the compounded drug cannot be assured.
JD & SN Inc. is recalling specific vials of Chorionic Gonadotropin because the FDA cannot assure the sterility of the compounded drug.
JD & SN Inc. is recalling 90 mg testosterone pellets because the agency could not ensure the sterile compounded drugs were sterile.
Moses Lake Professional Pharmacy is recalling Testosterone Cypionate for Subcutaneous Injection because the product lacks assurance of sterility.
The FDA is recalling 27 vials of Alprostadil/Procaine Injectable Solution because the manufacturer cannot ensure the product is sterile.
The FDA is recalling 834 syringes of Chorionic Gonadotropin compounded by Moses Lake Professional Pharmacy because the agency cannot ensure the product is sterile.
JD & SN Inc. is recalling six syringes of Trimix injectable solution because the company cannot guarantee the product's sterility.
JD & SN Inc. is recalling Estradiol pellets because the FDA determined there is a lack of assurance of sterility for all sterile human compounded drugs within their expiry.
American Pure Whey is recalling Whey Protein Matrix Chocolate flavor containers due to undeclared soy and milk allergens.
FDA is recalling Testosterone Cypionate for SubQ Injection from Moses Lake Professional Pharmacy due to lack of assurance of sterility.
Blue Bird is recalling certain school buses with Ricon wheelchair lifts where pivot holes may allow bearings to move, risking platform failure.
Kermit, Inc. is recalling 16-ounce bottles of Key Lime Barbecue Sauce due to undeclared soy on the label.
Pfizer is voluntarily recalling 21,120 bottles of Xanax (alprazolam) 0.25 mg tablets because the medication contains less active ingredient than labeled.