State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Tri-Coast Pharmacy is recalling 5,229 HCG 11,000 IU vials nationwide because the FDA cannot ensure the products are sterile.
Tri-Coast Pharmacy is recalling compounded Glutamine 25 mg/mL vials nationwide because the agency cannot assure the products are sterile.
Wells Pharmacy Network LLC is recalling 106 vials of a compounded injectable product due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 266 vials of compounded Testosterone Cypionate Injectable due to a lack of assurance of sterility.
Nurse Assist, Inc. is recalling Normal Saline Flush syringes due to potential contamination with B. cepacia. The affected products were distributed in the US, US Virgin Islands, and Canada.
Wells Pharmacy Network LLC is recalling 67 vials of Sodium Bicarbonate, 8.4% Injectable, due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 137 vials of compounded Glutamine/Arginine/Carnitine Injectable due to a lack of assurance of sterility. The product was distributed nationwide.
Wells Pharmacy Network LLC is recalling 199 vials of a compounded injectable product nationwide due to a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling 17 vials of Quad Mix compounded sterile drug due to a lack of assurance of sterility. The products were distributed nationwide.
Tri-Coast Pharmacy is recalling 265 vials of compounded BCAA solution because the agency cannot ensure the products are sterile.
Tri-Coast Pharmacy is recalling 278 vials of MIC Ultra Cocktail nationwide due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 122 syringes of Mitomycin Solution Injectable because the agency could not ensure the product was sterile.
Wells Pharmacy Network LLC is recalling compounded Testosterone Cypionate in Sesame Oil Injectable vials due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 16 vials of Dexamethasone Sodium Phosphate 24 mg/mL injectable due to a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling 141 vials of TriMix compounded injections nationwide due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling QUAD1 injectable vials because the FDA determined there is a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling Sermorelin Acetate/GHRP Injectable Kits nationwide because the agency cannot assure the product is sterile.
Wells Pharmacy Network LLC is recalling 1,753 kits of compounded Chorionic Gonadotropin injectable kits nationwide due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 21 vials of Testosterone Cypionate in Sesame Oil Injectable due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 648 vials of MIC/Chromium/B12(M) Injectable because the agency cannot assure the product is sterile.
Tri-Coast Pharmacy is recalling 1,544 vials of compounded Testosterone Cypionate/Zinc Gluconate in Sesame Oil nationwide due to a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling compounded Pyridoxine HCL 100 mg/ml vials because there is a lack of assurance of sterility.
Subaru is recalling specific model years of Baja, Impreza, Forester, Legacy, Outback, and Tribeca vehicles to replace passenger air bag inflators that may rupture in a crash.
Tri-Coast Pharmacy is recalling 1,567 vials of compounded Testosterone Enanthate in Sesame Oil due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 325 vials of Ultra-Test Injectable due to a lack of assurance of sterility. The product was distributed nationwide.