Living Free Heart/Blood Vessel Dietary Supplement — Class II food recall F-0777-2021
Terminated recall by Bea Lydeckers Naturals Inc, reported 2021-07-21, distributed nationwide. Label declares lecithin but does not declare soy lecithin.
| Recall number | F-0777-2021 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bea Lydeckers Naturals Inc, Oregon City, OR, United States |
| Recall initiated | 2021-06-21 |
| Classified | 2021-07-14 |
| Reported by FDA | 2021-07-21 |
| Terminated | 2022-02-24 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
Product
Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bottle. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Heart/Blood Vessel Dietary Supplement***Glandular Herbal & Vitamin Blend***Formulated by Beatrice Lydecker ***Manufactured by Bea Lydecker's Naturals Oregon City, OR*** 503-631-8589***".
Reason for recall
Label declares lecithin but does not declare soy lecithin.
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-0777-2021. 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.