State
73,738 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,821 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 1,485 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Red Mountain Compounding Pharmacy is recalling S-Methylcobalamin 25mg/mL injections because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Methylcobalamin injections due to a lack of assurance of sterility. The recall covers 60 vials distributed nationwide.
Red Mountain Compounding Pharmacy is recalling S-SOD Citrate 4% Injection due to a lack of assurance of sterility. The affected product was distributed nationwide.
Red Mountain Compounding Pharmacy is recalling specific lots of S-Lidocaine HCl 1% vials because the FDA identified a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific lots of S-Edetate Disodium 15% Injection because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific lots of 3% hydrogen peroxide vials due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Progesterone/Testosterone 0.05%/0.03% Oil Opth due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific lots of S-Cyanocobalamin 1,000 mcg/mL injection solution because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-MIC 25/50/50mg/mL B12 1mg/mL MDV Injection Solution vials because of a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Methylcobalamin 5,000mcg/mL injections because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Folic Acid 10mg/ml injection vials due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Vit B Complex Injection vials due to a lack of assurance of sterility. The product was distributed nationwide in the USA.
Red Mountain Compounding Pharmacy is recalling S-Procaine HCL 1% Buffered MDV vials because the FDA determined there is a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Gentamicin 480mg/1L irrigation solution because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-DMPS 50mg/ml injection vials because the FDA identified a lack of assurance of sterility.
Mylan Pharmaceuticals is recalling Alprazolam 0.5 mg tablets because they contain a foreign substance. Consumers should stop using the affected lot and contact their pharmacist.
Red Mountain Compounding Pharmacy is recalling specific lots of S-TEST CYP/NAN-DECA 200/50MG/ML MDV in sesame oil because the agency could not ensure the product was sterile.
First Royal Care Co. LLC is recalling S-TRIMIX compounded injections nationwide due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific lots of S-Calcium Gluconate 10% Injection due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Test Cyp/Prop/Deca-Nan 250mg/ml vials because the FDA determined there is a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling 81 vials of S-Ascorbic Acid 500mg/mL due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Edetate Calcium 300mg/mL injection vials because the FDA identified a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-TRIMIX injection vials because the FDA determined there is a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Amitriptyline 10mg/mL injection vials because the FDA determined there is a lack of assurance of sterility.
Philips is recalling 1,167 Forte Gamma Camera Systems because a detector may fall unimpeded vertically to the end stops of its travel limit.