Drug recall
Human Chorionic Gonadotropin 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054…
FDA recall event 81629 · Class II · Pharm D Solutions, LLC
Key facts
| Event ID | 81629 |
|---|---|
| Recall numbers | D-0343-2019 |
| Recalling firm | Pharm D Solutions, LLC |
| Product type | Drugs |
| Products | 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 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile. |
| Initiation date | Nov 19, 2018 |
| Report date | Dec 26, 2018 |
| Termination date | Oct 13, 2020 |
| City | Houston |
| State | TX |
| Country | United States |
| FEI number | 3011043554 |
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.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: