Food Recall Check
Class II · Moderate risk Terminated Initiated May 8, 2015 (11 years ago)

250cc White Plastic Container containing 120 capsules recall

Recalled by Natural Creations Inc · Woodbine, IA, United States

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

Why it was recalled

Natural Creations announces allergy alert and voluntary recall of New Zealand Colostrum dietary supplement due to unidentified allergen inclusion (milk).

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

250cc White Plastic Container containing 120 capsules, labeled Natural Creations New Zealand Colostrum, Colostrum Supplement, MFG. FOR: Natural Creations, Woodbine, IA 51579, 712-647-1600

Quantity: 399 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.

Lot numbers: 1112301 (exp. 1/15) and 3102914 (exp. 2/17), all products with all expiration dates.

Where it was sold

Nationwide.

Virginia

FDA's distribution note: Distributed to 29 retailers nationwide. No foreign, government/military/VA accounts.

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. 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
Natural Creations Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
May 8, 2015
In FDA report of
Jun 17, 2015
Terminated
Dec 3, 2015
FDA recall number
F-2418-2015 · event 71245
Official record
FDA enforcement report search

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