DrugNov 7, 2018
Pharm D Solutions Calcium Gluconate 2.5% a) 250 mL 25 mg/mL NDC 69699-0908-25 recall — FDA D-0149-2019
Lack of Assurance of Sterility
Class IIIFDA: TerminatedPharm D Solutions, LLC
Recall history in this database
Classification mix: Class III: 3.
DrugJan 18, 2017
Pharm D Solutions HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial recall — FDA D-0427-2017
Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct
Class IIIFDA: TerminatedPharm D Solutions, LLC
DrugJan 18, 2017
Pharm D Solutions Testosterone Cypionate 200 mg/mL in Sesame Oil, 4 mL and 5 mL vials recall — FDA D-0426-2017
Incorrect/Undeclared Excipient; product description section of testosterone cypionate incorrectly states "in grapeseed oil" instead of "in sesame oil" . The primary panel is correct
Class IIIFDA: TerminatedPharm D Solutions, LLC
Understanding this recall history
This page summarizes recall records in which the official source identifies Pharm D Solutions, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.