State
73,827 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,823 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,494 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,827 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 92 testosterone pellets because the company cannot ensure they are sterile. The recall covers products distributed nationwide.
FDA is recalling Testosterone/Anastrozole pellets from Moses Lake Professional Pharmacy because the agency cannot ensure the sterile compounded drugs are sterile.
JD & SN Inc. is recalling Testosterone/Anastrozole pellets because the FDA identified a lack of assurance of sterility for the compounded drugs.
JD & SN Inc. is recalling 8 syringes of Dihydroergotamine Mesylate Injectable Solution due to a lack of assurance of sterility.
JD & SN Inc. is recalling Hydroxocobalamin syringes because the FDA cannot assure the products are sterile.
Moses Lake Professional Pharmacy is recalling compounded Testosterone Cypionate injectable solution due to a lack of assurance of sterility.
American Pure Whey is recalling Whey Protein Isolate (Chocolate flavor) in 2 lb. and 5 lb. containers due to undeclared soy and milk allergens.
JD & SN Inc. is recalling Methylcobalamin MDV Injectable Solution due to a lack of assurance of sterility. The recall covers all sterile human compounded drugs within their expiry dates.
JD & SN Inc. is recalling 25 mg testosterone pellets because the agency cannot ensure the sterile compounded drugs are free from contamination.
Welch Allyn is recalling KleenSpec Corded Illuminators because they may be connected to AC power, posing a shock hazard.
American Pure Whey is recalling Whey Protein Isolate (Vanilla flavor) due to undeclared soy and milk allergens.
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.