Swanson — Class III food recall F-0220-2014
Terminated recall by Swanson Health Products, Inc, reported 2013-11-27, distributed nationwide. Swanson Health Products is recalling two lots of Swanson Premium Full Spectrum Black Cumin Seed (Nigella sativ
| Recall number | F-0220-2014 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Swanson Health Products, Inc, Fargo, ND, United States |
| Recall initiated | 2013-09-26 |
| Classified | 2013-11-20 |
| Reported by FDA | 2013-11-27 |
| Terminated | 2014-06-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BH, DK, FR, GB, HK, IE, IL, JP, PL, PT, TH, TW |
| Quantity | 3,689 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00087614113616 |
Product
Swanson, Premium Brand, Full Spectrum Black Cumin Seed (Nigella Sativa) Dietary Supplement capsules, 400 mg, SW1361, UPS 0 87614 11361 6.
Reason for recall
Swanson Health Products is recalling two lots of Swanson Premium Full Spectrum Black Cumin Seed (Nigella sativa) Dietary Supplement Capsules. The product was found to be mislabel. Bottles of Black Cumin Seed from these two lots numbers (199399 & 201359) have been found to contain White Cumin Seed (Cuminum cyminum).
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-0220-2014. 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.