Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bottle. Product is packed in white, HDPE pl
Summary
The FDA issued a Class II for Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bott by Bea Lydeckers Naturals Inc. Reason: Label declares lecithin but does not declare soy lecithin..
Details
Source
Food Recall
External ID
F-0777-2021
Action Date
2021-07-21
Status
Terminated
Category
food
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***".
Lot/Code Info: No lot code or expiration date listed on label.
Quantity Affected: Firm did not provide
Reason for Recall
Label declares lecithin but does not declare soy lecithin.
Distribution
distributed nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-06-21
Company
Oregon City, OR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Bea Lydeckers Naturals Inc has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Bea Lydeckers Naturals Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bea Lydeckers Naturals Inc have FDA actions?
Bea Lydeckers Naturals Inc has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0777-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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