Food Recall Check
Class I · High risk Terminated Initiated Jun 23, 2016 (10 years ago)

Michael's Naturopathic Programs Cholesterol Metabolism Factors recall

Recalled by Inner Health Group, Inc dba Michael's Naturopathic Programs · San Antonio, TX, United States

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

Why it was recalled

May contain undeclared milk (in the form of calcium caseinate) and soy.

Undeclared allergens: Milk Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Michael's Naturopathic Programs Cholesterol Metabolism Factors 270 count, 180 count, and 90 count tablets packaged in plastic bottles

Quantity: 18,375 units

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.

Lot numbers: 1307013, 1310060, 1402177, 1405356, 1408114, 1410186, 1501476, 1505367, 1510296, 1602062

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

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. The risk from an undeclared allergen is to people allergic to milk, soy; for anyone else the product is generally not a safety concern. 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
Inner Health Group, Inc dba Michael's Naturopathic Programs
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 23, 2016
In FDA report of
Aug 10, 2016
Terminated
Dec 16, 2016
FDA recall number
F-1869-2016 · event 74517
Official record
FDA enforcement report search

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