¿Topicort — Class III drug recall D-0950-2016
Terminated recall by Taro Pharmaceuticals U.S.A., Inc., reported 2016-06-08, distributed in CA, CT, MA, MD, NJ, NY, OK, TX…. Subpotent Drug
| Recall number | D-0950-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY, United States |
| Recall initiated | 2016-03-31 |
| Classified | 2016-05-31 |
| Reported by FDA | 2016-06-08 |
| Terminated | 2018-06-06 |
| Distributed | CA, CT, MA, MD, NJ, NY, OK, TX, WA |
| Quantity | 62,800 tubes |
| Reason classes | potency |
| NDC | 51672-5205-05 |
| Lot numbers | A5192-18338 |
| Expiration dates | 2016-12 |
Product
¿Topicort (desoximetasone) Cream USP, 0.05%, Packaged in 5 g Tubes, Professional Sample Only, Rx Only. Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: TaroPharma a division of Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532. NDC: 51672-5205-5.
Reason for recall
Subpotent Drug
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-0950-2016. 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.