Item FG 10149 — Class III food recall F-1367-2019
Terminated recall by Barlean's Llc, reported 2019-05-22, distributed nationwide. Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods
| Recall number | F-1367-2019 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Barlean's Llc, Ferndale, WA, United States |
| Recall initiated | 2019-05-06 |
| Classified | 2019-05-16 |
| Reported by FDA | 2019-05-22 |
| Terminated | 2020-10-15 |
| Distributed | Nationwide (US) |
| Quantity | 1,360 bottles |
| Reason classes | undeclared allergen, chemical contamination |
| UPC / GTIN / UDI-DI | 00705875100199 |
| Model numbers | 10149 |
| Expiration dates | 2022-01-20 |
Product
Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle, UPC 7 05875 10019 9
Reason for recall
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
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-1367-2019. 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.