Living Free Heart/Blood Vessel Dietary Supplement recall

Recalled by Bea Lydeckers Naturals Inc · Oregon City, OR, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Label declares lecithin but does not declare soy lecithin.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What 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***".

Quantity: Firm did not provide

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

No lot code or expiration date listed on label.

Where it was sold

Nationwide.

FDA's distribution note: distributed nationwide.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Bea Lydeckers Naturals Inc
Initiated by: Voluntary: Firm initiated
Recall initiated: Jun 21, 2021
In FDA report of: Jul 21, 2021
Terminated: Feb 24, 2022
FDA recall number: F-0777-2021 · event 88142
Official record: FDA enforcement report search

Also recalled with it (5 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Labeling Jun 21, 2021