Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported July 21, 2021
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***".
Label declares lecithin but does not declare soy lecithin.
Bea Lydeckers Naturals Inc recalled Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bottle. Prod… — a moderate-severity action.
Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bottle. Prod… was recalled by Bea Lydeckers Naturals Inc in July 21, 2021. Reason: Label declares lecithin but does not declare soy lecithin.. Check the official notice for the remedy. Verify recall #F-0777-2021 with the FDA Food before acting.
The recall
Bea Lydeckers Naturals Inc issued this moderate-severity FDA Food recall — Label declares lecithin but does not declare soy lecithin..
- Moderate
- severity level
- Class II
- classification
- July 21, 2021
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0777-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0777-2021) was formally reported on July 21, 2021, with the manufacturer initiating the action on June 21, 2021. It is classified under Moderate severity (Class II), with a current status of Terminated. Bea Lydeckers Naturals Inc is listed as the recalling firm, operating out of Oregon City, OR. Federal records list the affected scope as Firm did not provide.
The documented reason for this recall is: Label declares lecithin but does not declare soy lecithin. Distribution data in the federal record shows the product reached: distributed nationwide.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 1 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category — 14,048 drugs & medications recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.
Affected scope
Firm did not provide
Related Recalls
6
1 from same agency
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0777-2021 |
| Date reported | July 21, 2021 |
| Date initiated | June 21, 2021 |
| Recalling firm | Bea Lydeckers Naturals Inc |
| Firm location | Oregon City, OR |
| Affected scope | Firm did not provide |
| Distribution | distributed nationwide. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0777-2021) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting — recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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***".. Recalled by Bea Lydeckers Naturals Inc. Units affected: Firm did not provide.
Why was this product recalled? ▼
Label declares lecithin but does not declare soy lecithin.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on July 21, 2021. Severity: Moderate. Recall number: F-0777-2021.
Where was the recalled product distributed? ▼
Distribution: distributed nationwide..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0777-2021) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported July 21, 2021.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.