PlainRecalls
FDA Drug Moderate Class II Terminated

HCG 20 Day Injection, 2625 Units/4 mL, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

Reported: April 24, 2019 Initiated: April 2, 2019 #D-1148-2019

Product Description

HCG 20 Day Injection, 2625 Units/4 mL, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

Reason for Recall

Lack of sterility assurance.

Details

Units Affected
217 vials
Distribution
Nationwide
Location
Bristol, TN

Frequently Asked Questions

What product was recalled?
HCG 20 Day Injection, 2625 Units/4 mL, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.. Recalled by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy. Units affected: 217 vials.
Why was this product recalled?
Lack of sterility assurance.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 24, 2019. Severity: Moderate. Recall number: D-1148-2019.