Drug recall

Human Chorionic Gonadotropin 11000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL…

FDA recall event 80699 · Class II · Pharmcore Inc.

Key facts

Event ID 80699
Recall numbers D-1147-2018, D-1148-2018, D-1149-2018, D-1150-2018, D-1151-2018, D-1152-2018, D-1153-2018, D-1154-2018, D-1155-2018
Recalling firm Pharmcore Inc.
Product type Drugs
Products Human Chorionic Gonadotropin 11000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009, Human Chorionic Gonadotropin 20000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009, Human Chorionic Gonadotropin 2500 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009, Human Chorionic Gonadotropin 4000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009, Human Chorionic Gonadotropin 5000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009 and 4 more
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Lack of assurance of sterility.
Initiation date Aug 2, 2018
Report date Sep 5, 2018
Termination date Jan 18, 2022
City Hallandale Beach
State FL
Country United States
FEI number 3014480778

At a glance

  • 1–9 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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