FDA (Drugs) recall action 71806
The FDA (Drugs) publishes a recall like this one as 101 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 101 pages.
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
The agency’s own wording, quoted from the enforcement report.
The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.
JD & SN Inc. is recalling 5 syringes of Testosterone Propionate Injectable Solution due to a lack of assurance of sterility.
JD & SN Inc. is recalling Estradiol 18 mg pellets because the company cannot assure the sterility of the product. The recall covers all sterile human compounded drugs within their expiry date.
The FDA is recalling 9 vials of Chorionic Gonadotropin Injectable Solution from Moses Lake Professional Pharmacy due to a lack of assurance of sterility.
The FDA is recalling Estradiol pellets from JD & SN Inc. because the manufacturer cannot ensure the sterile compounded drugs are free of contamination.
JD & SN Inc. is recalling 6 syringes of Dexpantenol Injectable Solution because the FDA identified a lack of assurance of sterility.
JD & SN Inc. is recalling TRIMIX injectable solution because the agency could not ensure the product remained sterile. Patients should stop using the medication and contact their healthcare provider.
JD & SN Inc. is recalling 95 vials of Chorionic Gonadotropin because the FDA could not verify the sterility of the compounded drug.
Moses Lake Professional Pharmacy is recalling Estradiol Pellets because the FDA determined there is a lack of assurance of sterility for the compounded drug.
JD & SN Inc. is recalling 298 units of compounded testosterone pellets because the FDA cannot ensure the product is sterile.
The FDA is recalling 36 syringes of Methylcobalamin Injectable Solution because the manufacturer cannot ensure the product is sterile.
JD & SN Inc. is recalling a compounded injectable solution because the FDA could not ensure the product remained sterile. Patients should stop using the medication and contact their healthcare provider.
Moses Lake Professional Pharmacy is recalling 355 testosterone pellets because the FDA cannot assure they are sterile. Patients should stop using the product and consult a healthcare provider.
JD & SN Inc. is recalling 8 syringes of Vitamin D3 Oil Injectable Solution due to a lack of assurance of sterility.
FDA is recalling a compounded injectable solution due to a lack of assurance of sterility. The product is distributed nationwide.
The FDA is recalling Estradiol pellets compounded by Moses Lake Professional Pharmacy because the firm cannot assure the sterility of the product.
Moses Lake Professional Pharmacy is recalling 30 syringes of compounded injectable cyanocobalamin because the product lacks assurance of sterility.
JD & SN Inc. is recalling 15 syringes of Trimix injectable solution because the FDA could not assure the sterility of the compounded drug.
JD & SN Inc. is recalling Hydroxocobalamin Injectable Solution because the agency cannot ensure the product is sterile. Patients should stop using the product and contact their healthcare provider.
The FDA is recalling 6 syringes of Pyridoxine HCL injectable solution from JD & SN Inc. due to a lack of assurance of sterility.
Moses Lake Professional Pharmacy is recalling compounded chorionic gonadotropin injectable solutions because the FDA cannot assure the sterility of the product.
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.