250cc White Plastic Container containing 120 capsules
Reason Natural Creations announces allergy alert and voluntary recall of New Zealand Colostrum dietary supplement due to unidentified allergen inclusion (milk).
Natural Creations Glucosamine MSM 90 capsules packaged in 250 cc… 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 is recalling Glucosamine MSM dietary supplement due to unlabeled allergen (shellfish).
Undeclared allergen: Shellfish
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
Natural Creations Glucosamine MSM 90 capsules packaged in 250 cc white plastic containers with 52 bottles per case.
Quantity: 644 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: 4072202, 3073009, 2030110, 1010705. All products with expiration dates.
Where it was sold
Nationwide.
Virginia
FDA's distribution note: Nationwide. No foreign/VA/govt/military.
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 shellfish; 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 4, 2015
- In FDA report of
- Jul 1, 2015
- Terminated
- Dec 3, 2015
- FDA recall number
- F-2767-2015 · event 71249
- Official record
- FDA enforcement report search
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