Q-min — Class II food recall F-0182-2020
Terminated recall by Basic Reset Inc., reported 2019-11-27, distributed nationwide. Products do not conform to Dietary Supplement CGMP regulations.
| Recall number | F-0182-2020 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Basic Reset Inc., Hendersonville, TN, United States |
| Recall initiated | 2019-09-23 |
| Classified | 2019-11-21 |
| Reported by FDA | 2019-11-27 |
| Terminated | 2020-08-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, GB, GR, HU, IL, MX, NG, PH |
| Reason classes | cgmp |
Product
Q-min, 50 capsules per plastic bottle, SKU: 100-9B
Reason for recall
Products do not conform to Dietary Supplement CGMP regulations.
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/F-0182-2020. 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.