screamin' menthol — Class II drug recall D-0835-2018
Terminated recall by Ideaz Llc, reported 2018-05-30, distributed nationwide. CGMP Deviations: Products manufactured with an ingredient that exceed the benzene levels allowed in drug produ
| Recall number | D-0835-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ideaz Llc, Mc Kees Rocks, PA, United States |
| Recall initiated | 2018-05-16 |
| Classified | 2018-05-24 |
| Reported by FDA | 2018-05-30 |
| Terminated | 2018-11-06 |
| Distributed | Nationwide (US) |
| Quantity | 800 pounds |
| Reason classes | chemical contamination, cgmp |
| UPC / GTIN / UDI-DI | 00750263800069, 00750263800625, 00750263800663 |
| Lot numbers | 10/18, 1015019, 11/19, 1116011 |
Product
screamin' menthol (menthol) Pain Relieving Gel, 4%, packaged in a) 2 OZ (57g) tubes, UPC 7 50263 80062 5; b) 5 oz. (141g) tubes, UPC 7 50263 80006 9; and c) 16 oz. (454g) bottles, UPC 7 50263 80066 3; MFD FOR: Toast Products, 400 Sproul Street, Pittsburgh, PA 15136; NDC 52099-8010.
Reason for recall
CGMP Deviations: Products manufactured with an ingredient that exceed the benzene levels allowed in drug products.
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-0835-2018. 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.