State
73,833 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,635 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,567 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The FDA is recalling specific lots of compounded testosterone pellets from Moses Lake Professional Pharmacy because the manufacturer cannot ensure the products are sterile.
JD & SN Inc. is recalling 42 syringes of Chorionic Gonadotropin/Cyanocobalamin Injectable Solution due to a lack of assurance of sterility.
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling Methylcobalamin Injectable Solution because the agency cannot assure the sterility of the compounded drug.
FDA is recalling specific lots of compounded testosterone pellets because they lack assurance of sterility. Patients should contact their healthcare provider.
JD & SN Inc. is recalling 116 mg testosterone pellets because the agency could not ensure the sterile compounded drugs were sterile.
FDA is recalling 64 syringes of compounded chorionic gonadotropin from Moses Lake Professional Pharmacy due to lack of assurance of sterility.
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 30 mL vials of an injectable solution containing vitamins, lidocaine, and other compounds due to a lack of assurance of sterility.
JD & SN Inc. is recalling 5 syringes of Hydroxocobalamine/Methylcobalamine Injectable Solution due to a lack of assurance of sterility.
JD & SN Inc. is recalling specific vials of Chorionic Gonadotropin injectable solution because the agency could not ensure the sterile human compounded drugs were sterile.
JD & SN Inc. is recalling specific syringes of Methylcobalamin Injectable Solution because the FDA cannot assure the sterility of the compounded drug.
JD & SN Inc. is recalling 184 syringes of compounded chorionic gonadotropin nationwide because the FDA could not ensure the product was sterile.
FDA is recalling Alprostadil Injectable Solution vials from Moses Lake Professional Pharmacy because the agency cannot assure the sterility of the compounded drug.
JD & SN Inc. is recalling EDETATE CALCIUM DISODIUM Injectable Solution due to a lack of assurance of sterility.
JD & SN Inc. is recalling 50 mg testosterone pellets because the FDA cannot ensure the sterile compounded drugs are free from contamination.
Moses Lake Professional Pharmacy is recalling 11 syringes of Medroxyprogesterone Acetate because the FDA determined there is a lack of assurance of sterility.
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.