Food Recall Check
Class I · High risk Terminated Initiated Aug 26, 2016 (10 years ago)

Dietary Supplement Acidophilus Blend recall

Recalled by Complete Packaging & Manufacturing, LLC · Orem, UT, United States

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

Why it was recalled

Nature's Power Solutions Acidophilus Blend due to undeclared milk allergen.

Undeclared allergen: Milk

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

Dietary Supplement Acidophilus Blend, 90 capsules, Product No. E-420, packaged in 225cc HDPE white bottle, room temp, sold individually

Quantity: 1327 bottles

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.

12/28/15 Lot# 24553-295 bottles 3/18/16 Lot# 24631 -328 bottles 5/10/16 Lot# 24674 -344 bottles 7/28/16 Lot# 24774 -360 bottles

Where it was sold

Nationwide.

Virginia

FDA's distribution note: nationwide. No foreign or govt/military/VA consignees.

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; 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
Complete Packaging & Manufacturing, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 26, 2016
In FDA report of
Oct 19, 2016
Terminated
May 31, 2017
FDA recall number
F-0049-2017 · event 75151
Official record
FDA enforcement report search

Recent dietary supplements recalls

All dietary supplements recalls