Triamcinolone Acetonide cream — Class II drug recall D-1535-2022
Completed recall by Direct Rx, reported 2022-09-21, distributed in GA, ID. CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness.
| Recall number | D-1535-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Direct Rx, Dawsonville, GA, United States |
| Recall initiated | 2022-09-12 |
| Classified | 2022-09-15 |
| Reported by FDA | 2022-09-21 |
| Distributed | GA, ID |
| Quantity | 20 tubes |
| Reason classes | cgmp |
| NDC | 72189-0330, 72189-0330-80 |
| Lot numbers | 12JY2216 |
| Expiration dates | 2024-02-29 |
Product
Triamcinolone Acetonide cream, 0.1%, 80 g tube, Rx only, Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534, Dist. By Perrigo, Allegan, MI 49010, NDC 72189-330-80.
Reason for recall
CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness.
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-1535-2022. 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.