Pharmcore product recalled over sterility concerns
- Recall date
- August 2, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Pharmcore Inc. recalls Human Chorionic Gonadotropin 2500 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009
- Recall number
- D-1150-2018
- FDA classification
- Class II
- Brand / firm
- Pharmcore Inc.
- Sold / distributed
- Nationwide
Why it was recalled
Lack of assurance of sterility.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Human Chorionic Gonadotropin 2500 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009
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