Food Recall Check
Class I · High risk Terminated Initiated Dec 23, 2021 (5 years ago)

Moor Herbs Healthy Beauty Angel Formula packed in recall

Recalled by Moor Herbs · Detroit, MI, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product is marketed as an infant formula but the required pre-market infant formula notification for this product has not been submitted to the FDA. Product tested by FDA was well above the maximum acceptable range for Iron, Potassium and Sodium, which could potentially lead to iron overload and/or electrolyte imbalances. In addition, the product did not have vitamin D, and a vitamin D deficiency can potentially lead to rickets, a softening and weakening of bones.

Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.

What was recalled

Moor Herbs Healthy Beauty Angel Formula packed in 16oz. plastic containers

Quantity: 147 units

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.

All products. Product does not have any lot code information.

Where it was sold

FDA's distribution note: Products were distributed via internet sales and through the firm's store-front.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Moor Herbs
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 23, 2021
In FDA report of
Jan 19, 2022
Terminated
Aug 2, 2024
FDA recall number
F-0519-2022 · event 89299
Official record
FDA enforcement report search