Drug recall
Domperidone capsules 10 mg, compounded, dispensed in 60, 90, and 360 count bottles, Jeffreys Drug Store 1…
FDA recall event 75741 · Class I · Jeffreys Drug Store
Key facts
| Event ID | 75741 |
|---|---|
| Recall numbers | D-0494-2017 |
| Recalling firm | Jeffreys Drug Store |
| Product type | Drugs |
| Products | Domperidone capsules 10 mg, compounded, dispensed in 60, 90, and 360 count bottles, Jeffreys Drug Store 1 North Central Ave. Canonsburg, PA |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Marketed without an approved NDA/ANDA for which safety and efficacy has not been established. |
| Initiation date | Nov 23, 2016 |
| Report date | Mar 8, 2017 |
| Termination date | Oct 29, 2018 |
| City | Canonsburg |
| State | PA |
| Country | United States |
| FEI number | 3012080718 |
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: