Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy recalls Heparin 20,000 U/Lidocaine 2% 10 mL/Sodium Bicarbonate 8.4% 10 mL/Sterile Water 5 mL, 27 mL Syringe, Anderson Compoundi…

Recall date

April 2, 2019

Source

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

Recall number

D-1156-2019

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 20,000 U/Lidocaine 2% 10 mL/Sodium Bicarbonate 8.4% 10 mL/Sterile Water 5 mL, 27 mL Syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.