Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy recalls DMSO 50% 60 mL/Heparin 1 mL/ Sodium Bicarbonate 60 mL/ Solu-Cortef 100 mg, 41 mL syringe, Anderson Compounding Pharmacy…

Recall date

April 2, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-1142-2019

FDA classification

Class II

Brand / firm

Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Sold / distributed

Nationwide

Why it was recalled

Lack of sterility assurance.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

DMSO 50% 60 mL/Heparin 1 mL/ Sodium Bicarbonate 60 mL/ Solu-Cortef 100 mg, 41 mL syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.