Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 2, 2014 (12 years ago)

PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle recall

Recalled by ReNew Life Formulas, Inc. · Palm Harbor, FL, United States

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

Why it was recalled

Labels indicate "no wheat" "no gluten" and the products contain gluten and wheat or a wheat related allergen.

Undeclared allergen: Wheat

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

PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle

Quantity: 55,271 bottles

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.

Product code: 17515, UPC code: 631257175151, Lot 49413, Exp. Date 8/2015 (Mfg date 8/20/2012); Lot 50854, Exp. Date 8/2015 (Mfg date 8/20/2012); Lot 50897, Exp. Date 8/2015 (Mfg. date 8/20/2012); Lot 51417, Exp. Date 10/2015 (Mfg. date 10/26/2012); Lot 52531, Exp. Date 10/2015 (Mfg. date 10/26/2012); Lot 53635, Exp. Date 12/2015 (Mfg. date 12/12/2012)

Where it was sold

Alaska Alabama Arkansas Arizona California Colorado Connecticut Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin West Virginia Wyoming

FDA's distribution note: GA, NC, SC, MD, VA, WV, IL, OH, KY, AR, OK, TX, CO, NM, WY, UT, IN, MI, FL, KS, IA, MO, NE, CA, AZ, MN, ND, SD, WI, CT, MA, ME, NH, RI, VT, NJ, AL, LA, MS, TN, NY, DE, PA, NV, AK, ID, MT, OR, WA, Hawaii and Puerto Rico

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 wheat; 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
ReNew Life Formulas, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 2, 2014
In FDA report of
Apr 22, 2015
Terminated
Mar 2, 2017
FDA recall number
F-1946-2015 · event 70156
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.