HCG inj multidose vial compounded recalled over sterility concerns

Recall date

April 8, 2019

Source

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

Official notice title

Customceutical Compounding recalls HCG (CHORIONIC GONADOTROPIN 1000 IU/ML PEP 25 mg/mL) inj 5 mL multidose vial compounded. Customceutical Compounding 461…

Recall number

D-1256-2019

FDA classification

Class II

Brand / firm

Customceutical Compounding

Sold / distributed

U.S.A. Nationwide

Why it was recalled

Lack of assurance of sterility for injectables and solutions intended to be sterile.

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

What was recalled

HCG (CHORIONIC GONADOTROPIN 1000 IU/ML PEP 25 mg/mL) inj 5 mL multidose vial compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272