Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy recalls Heparin 20,000U/Marcaine 0.25%, 10 mL, Sodium Bicarbonate 8.4% 48 mL, 60 mL Syringe, Anderson Compounding Pharmacy 310…

Recall date

April 2, 2019

Source

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

Recall number

D-1191-2019

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

Heparin 20,000U/Marcaine 0.25%, 10 mL, Sodium Bicarbonate 8.4% 48 mL, 60 mL Syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.