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Pharm D Solutions Recalls
100 recalls on record · January 18, 2017 to June 19, 2019 · Drugs
Recalls by year
17
18
19
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 7, 2018DrugsFDA
Pharm D Solutions, LLC recalls Bi-Mix Injection (Alprostadil 80 mcg/Lidocaine 2 mg/mL) Pharm D Solutions, Houston, Texas --- NDC 69699-1317-03
Hazard: Lack of Assurance of Sterility
November 7, 2018DrugsFDA
Pharm D Solutions, LLC recalls Bi-Mix Injection, (Alprostadil 40 mcg/Lidocaine 2 mg/mL) Pharm D Solutions, Houston, Texas --- NDC 69699-1305-03
Hazard: Lack of Assurance of Sterility
November 7, 2018DrugsFDA
Pharm D Solutions, LLC recalls Bi-Mix Injection (Alprostadil 150 mcg/Lidocaine 2 mg/mL), Pharm D Solutions, Houston, Texas --- NDC 69699-1323-05
Hazard: Lack of Assurance of Sterility
November 7, 2018DrugsFDA
Pharm D Solutions, LLC recalls Bacteriostatic Water for Injection 10 mL, Pharm D Solutions, Houston, Texas --- NDC 69699-1417-10
Hazard: Lack of Assurance of Sterility
November 7, 2018DrugsFDA
Pharm D Solutions, LLC recalls Beta-complex B-1, B-6, B-3, B-12, B-5 100, 2.54 Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1611-30
Hazard: Lack of Assurance of Sterility
November 7, 2018DrugsFDA
Pharm D Solutions, LLC recalls Ascorbic Acid 500 mg/mL Solution Pharm D Solutions, Houston, Texas --- NDC 69699-1502-50
Hazard: Lack of Assurance of Sterility
November 7, 2018DrugsFDA
Pharm D Solutions, LLC recalls Arginine Injections 100 mcg/mL, Pharm D Solutions, Houston, Texas NDC 69699-1414-20
Hazard: Lack of Assurance of Sterility
November 7, 2018DrugsFDA
Pharm D Solutions, LLC recalls Acetylcysteine Injection 10 mg/5 mL (2 mg/mL), Pharm D Solutions, Houston, Texas ---- NDC 69699-1424-10
Hazard: Lack of Assurance of Sterility
January 18, 2017DrugsFDA
Pharm D Solutions, LLC recalls HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial, Rx only, For Sub-Q & IM Injection, Pharm D Solutions, Loop West Houston, TX
Hazard: Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct
January 18, 2017DrugsFDA
Pharm D Solutions, LLC recalls Testosterone Cypionate 200 mg/mL in Sesame Oil, 4 mL and 5 mL vials, Rx only, For IM injection, Pharm D Solutions, Loop
Hazard: Incorrect/Undeclared Excipient; product description section of testosterone cypionate incorrectly states "in grapeseed oil" instead of "in sesame oil" . The primary panel is correct