CORTISOL-MC — Class III drug recall D-1231-2015
Terminated recall by Abrams Royal Pharmacy II, LLC, reported 2015-07-15, distributed in TX. Failed Content Uniformity Specifications: Failed Uniformity of Dosage Units specifications.
| Recall number | D-1231-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Abrams Royal Pharmacy II, LLC, Plano, TX, United States |
| Recall initiated | 2015-06-23 |
| Classified | 2015-07-08 |
| Reported by FDA | 2015-07-15 |
| Terminated | 2017-01-13 |
| Distributed | TX |
| NDC | 88888-0043-31 |
| Expiration dates | 2015-09-28 |
Product
CORTISOL-MC, 10mg CAP, packaged in 30 and 90 count bottles, Rx Only, ABRAMS ROYAL pharmacy II, 4909 W Park Blvd, Suite 177, Plano, TX 75093 --- NDC 88888-0043-31
Reason for recall
Failed Content Uniformity Specifications: Failed Uniformity of Dosage Units specifications.
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-1231-2015. 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.