Manufacturer
101 recalls in our database name JD & SN Inc., dba Moses Lake Professional Pharmacy as the manufacturing or recalling firm.
Of the 101 recalls from JD & SN Inc., dba Moses Lake Professional Pharmacy we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 100 (99%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
The FDA is recalling Estradiol 12 mg pellets from Moses Lake Professional Pharmacy because the manufacturer cannot ensure the sterile compounded drugs are sterile.
FDA is recalling 100 syringes of Sodium Tetradecyl Sulfate Injectable Solution 3% due to lack of assurance of sterility.
JD & SN Inc. is recalling six syringes of Trimix injectable solution because the company cannot guarantee the product's 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 compounded progesterone pellets from JD & SN Inc. because the manufacturer cannot guarantee the products are sterile.
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 8 syringes of Vitamin D3 Oil Injectable Solution due to a lack of assurance of sterility.
FDA is recalling Testosterone Cypionate for SubQ Injection from Moses Lake Professional Pharmacy due to 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 Hydroxocobalamin syringes because the FDA cannot assure the products 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.
JD & SN Inc. is recalling 91 vials of compounded testosterone pellets because the FDA cannot assure the sterility of the product.
JD & SN Inc. is recalling 15 syringes of Trimix injectable solution because the FDA could not assure the sterility of the compounded drug.
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 155 syringes of TRIMIX injectable solution nationwide due to a lack of assurance of sterility.
Moses Lake Professional Pharmacy is recalling Estradiol 25 mg pellets because the agency cannot assure the sterility of the compounded drug.
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 compounded vitamin injectable solutions due to a lack of assurance of sterility.
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 Testosterone/Anastrozole pellets because the FDA identified a lack of assurance of sterility for the compounded drugs.
JD & SN Inc. is recalling 95 vials of Chorionic Gonadotropin because the FDA could not verify the sterility of the compounded drug.
JD & SN Inc. is recalling 42 syringes of Chorionic Gonadotropin/Cyanocobalamin Injectable Solution due to a lack of assurance of sterility.
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 184 syringes of compounded chorionic gonadotropin nationwide because the FDA could not ensure the product was sterile.
The FDA is recalling 6 syringes of Pyridoxine HCL injectable solution from JD & SN Inc. due to a lack of assurance of sterility.