RECALL RECORD — CLASS IIRecall closedF-1945-2015/FDA enforcement

Purelife Naturals Adult Multi-plus Multi-vitamins & Minerals Plus Herbs, 60 Pure Caps Hdpe…

What you need to know

Class II
  • What happened

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

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAGA, NC, SC, MD +45 moreMore food

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Product identification

Source: FDA FOOD

Brand nameRenew Life Formulas, INC.
Recalling firmRenew Life Formulas, INC.Palm Harbor, FL, United States
UPC / barcodes
6 31257 17502 1
Lot / date codes
  • Product code: 17502, UPC code: 631257175021, Lot 49370, Exp. Date 8/2015 (Mfg date 8/7/2012)
  • Lot 50923, Exp. Date 8/2015 (Mfg date 8/7/2012)
  • Lot 51406, Exp. Date 10/2015 (Mfg. date 10/22/2012)
  • Lot 52401, Exp. Date 10/2015 (Mfg. date 10/22/2012)
  • Lot 57353, Exp. Date 12/2015 (Mfg. date 12/20/2012)
  • Lot 60265, Exp. Date 12/2015 (Mfg. date 12/20/2012)
Distribution area
GANCSCMDVAWVILOHKYAROKTXCONMWYUTINMIFLKSIAMONECAAZMNNDSDWICTMAMENHRIVTNJALLAMSTNNYDEPANVAKIDMTORWA

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

United States, Puerto Rico

Quantity affected60, 781 bottles
Recall initiationFDA report date: April 22, 2015
FDA recall numberF-1945-2015

Beyond the headline

The recall, in context

Renew Life Formulas, INC. initiated this food recall on December 2, 2014. The FDA enforcement report states: Labels indicate "no wheat" "no gluten" and the products contain gluten and wheat or a wheat related allergen. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: Labels indicate "no wheat" "no gluten" and the products contain gluten and wheat or a wheat related allergen.

Purelife Naturals Adult Multi-plus Multi-vitamins & Minerals Plus Herbs, 60 Pure Caps Hdpe… was made or distributed by Renew Life Formulas, INC. in Palm Harbor, FL, United States. This page reflects FDA report F-1945-2015, dated April 22, 2015.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared wheat or gluten

Symptoms to watch for

Wheat allergy can cause hives, nausea, cramps, breathing difficulty or anaphylaxis. For celiac disease, even small amounts of gluten can cause intestinal damage.

When symptoms may appear

Allergic reactions can begin within minutes to hours. Celiac-related intestinal effects may be delayed.

Higher-risk groups

People with wheat allergy, celiac disease, non-celiac gluten sensitivity or a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a wheat allergy or must avoid gluten.
  2. 2Seek emergency care for breathing difficulty or other signs of a severe allergic reaction.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Purelife Naturals Adult Multi-plus Multi-vitamins & Minerals Plus Herbs, 60 Pure Caps Hdpe… recall?

Renew Life Formulas, INC. recalled Purelife Naturals Adult Multi-plus Multi-vitamins & Minerals Plus Herbs, 60 Pure Caps Hdpe… in an FDA Class II enforcement action reported as F-1945-2015. Labels indicate "no wheat" "no gluten" and the products contain gluten and wheat or a wheat related allergen.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Do not eat the product if you have a wheat allergy or must avoid gluten. Seek emergency care for breathing difficulty or other signs of a severe allergic reaction. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Renew Life Formulas, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1945-2015. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Renew Life Formulas, INC.

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.