CHORIONIC GONADOTROPIN recalled over sterility concerns

Recall date

July 24, 2015

Source

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

Official notice title

JD & SN Inc., dba Moses Lake Professional Pharmacy recalls CHORIONIC GONADOTROPIN, Injectable Solution, 5000 UNITS/0.1 mL, vial sizes: 5 mL; 6 mL; 8 mL; 10 mL, Rx only, JD & SN I…

Recall number

D-0065-2016

FDA classification

Class II

Brand / firm

JD & SN Inc., dba Moses Lake Professional Pharmacy

Sold / distributed

Nationwide

Why it was recalled

Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

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

What was recalled

CHORIONIC GONADOTROPIN, Injectable Solution, 5000 UNITS/0.1 mL, vial sizes: 5 mL; 6 mL; 8 mL; 10 mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314