FDA Drug Recalls

Recalls / Class II

Class IID-1152-2018

Product

Human Chorionic Gonadotropin 6000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009

Affected lot / code info
Lots: HCG60122 Exp. 4/30/2019; HCG60124 Exp. 6/30/2019; HCG60121 Exp. 4/30/2019; HCG60123 Exp. 5/31/2019; HCG60120 Exp. 4/30/2019; HCG60118 Exp. 2/28/2019; HCG1115 Exp. 1/31/2019

Why it was recalled

Lack of assurance of sterility.

Recalling firm

Firm
Pharmcore Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1109 E Hallandale Beach Blvd, N/A, Hallandale Beach, Florida 33009-4431

Distribution

Quantity
3351 vials
Distribution pattern
Nationwide

Timeline

Recall initiated
2018-08-02
FDA classified
2018-08-28
Posted by FDA
2018-09-05
Terminated
2022-01-18
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1152-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls