Nature's Script CBD Cryotherapy Pain Relief Roll on — Class III drug recall D-0614-2024
Ongoing recall by GLOBAL WIDGET LLC, reported 2024-07-31, distributed nationwide. Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
| Recall number | D-0614-2024 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GLOBAL WIDGET LLC, Tampa, FL, United States |
| Recall initiated | 2024-06-25 |
| Classified | 2024-07-22 |
| Reported by FDA | 2024-07-31 |
| Distributed | Nationwide (US) |
| Quantity | 2,466 bottles |
| Reason classes | labeling, potency |
| UPC / GTIN / UDI-DI | 00840078567315 |
| Lot numbers | 230090, 230346 |
| Expiration dates | 2025-02-20, 2025-08-20 |
Product
Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, UPC code: 8-40078-56731-5
Reason for recall
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
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-0614-2024. 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.