Human Chorionic Gonadotropin 3000 IU recalled over sterility concerns
- Recall date
- November 19, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Pharm D Solutions, LLC recalls Human Chorionic Gonadotropin 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054 1-844-263-684…
- Recall number
- D-0343-2019
- FDA classification
- Class II
- Brand / firm
- Pharm D Solutions, LLC
- Sold / distributed
- WA
Why it was recalled
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
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 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054 1-844-263-6843 --- NDC: 69699-1738-10
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