PlainRecalls
FDA Drug Moderate Class II Terminated

CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 175 UNITS/0.175ML per syringe, packaged in 14, 26, and 40-count containers, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Reported: November 4, 2015 Initiated: July 24, 2015 #D-0067-2016

Product Description

CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 175 UNITS/0.175ML per syringe, packaged in 14, 26, and 40-count containers, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Reason for Recall

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

Details

Units Affected
1 (14-count) container, 1(40-count) container, 30 (26-count) container
Distribution
Nationwide
Location
Moses Lake, WA

Frequently Asked Questions

What product was recalled?
CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 175 UNITS/0.175ML per syringe, packaged in 14, 26, and 40-count containers, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314. Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy. Units affected: 1 (14-count) container, 1(40-count) container, 30 (26-count) container.
Why was this product recalled?
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Which agency issued this recall?
This recall was issued by the FDA Drug on November 4, 2015. Severity: Moderate. Recall number: D-0067-2016.