Domperidone capsules 10 mg — Class I drug recall D-0494-2017
Terminated recall by Jeffreys Drug Store, reported 2017-03-08, distributed in PA. Marketed without an approved NDA/ANDA for which safety and efficacy has not been established.
| Recall number | D-0494-2017 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Jeffreys Drug Store, Canonsburg, PA, United States |
| Recall initiated | 2016-11-23 |
| Classified | 2017-02-27 |
| Reported by FDA | 2017-03-08 |
| Terminated | 2018-10-29 |
| Distributed | PA |
| Reason classes | unapproved product |
| Lot numbers | 071116-103323 |
| Expiration dates | 2017-01-07 |
Product
Domperidone capsules 10 mg, compounded, dispensed in 60, 90, and 360 count bottles, Jeffreys Drug Store 1 North Central Ave. Canonsburg, PA
Reason for recall
Marketed without an approved NDA/ANDA for which safety and efficacy has not been established.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0494-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.