HYDROCORTISONE LOTION — Class III drug recall D-0859-2017
Terminated recall by Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals, reported 2017-05-31, distributed nationwide. Superpotent Drug: above specification for the assay.
| Recall number | D-0859-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals, Huntsville, AL, United States |
| Recall initiated | 2017-05-08 |
| Classified | 2017-05-23 |
| Reported by FDA | 2017-05-31 |
| Terminated | 2018-05-02 |
| Distributed | Nationwide (US) |
| Quantity | 109,620 bottles |
| Reason classes | potency |
| NDC | 00603-7785-52 |
| Lot numbers | 0000004961, 0000005197, 0000005198, 0000005199, 0000005200, 0000005201, 0000005202, 0000005203, 0000005204, 0000007022, 0000007998, 0000007999, 0000009176, 0000012281, 0000012282, 04/18, 05/17, 07/17, 09/17, 12/17, 12/18 |
Product
HYDROCORTISONE LOTION, USP, 2.5%, 2 FL OZ (59 mL) bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-7785-52.
Reason for recall
Superpotent Drug: above specification for the assay.
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-0859-2017. 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.