DaVinci Laboratories of Vermont Omega 3-1 — Class II food recall F-1595-2019
Terminated recall by FoodScience Corporation, reported 2019-07-31, distributed in AZ, CA, CT, FL, IL, IN, KS, LA…. Dietary supplement mislabeled, undeclared allergen.
| Recall number | F-1595-2019 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | FoodScience Corporation, Williston, VT, United States |
| Recall initiated | 2019-07-09 |
| Classified | 2019-07-23 |
| Reported by FDA | 2019-07-31 |
| Terminated | 2019-10-11 |
| Distributed | AZ, CA, CT, FL, IL, IN, KS, LA, MD, MI, MN, MO, NH, NY, OH, OR, VT |
| Countries outside the US | JP |
| Quantity | 256 bottles |
| Reason classes | undeclared allergen, labeling |
| UPC / GTIN / UDI-DI | 00026664273161 |
| Lot numbers | 35532200 |
| Expiration dates | 2022-05 |
Product
DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161
Reason for recall
Dietary supplement mislabeled, undeclared allergen.
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-1595-2019. 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.