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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food

ReNew Life Formulas, Inc.: Labels indicate "no wheat" "no gluten" and the products contain gluten and wheat or a wheat related allergen.

Agency Publication Date: April 10, 2015
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Affected Products

Product: PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle

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)

Lot Numbers:
17502
631257175021
49370
50923
51406
52401
57353
60265
Product: PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle

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)

Lot Numbers:
17515
631257175151
49413
50854
50897
51417
52531
53635

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 70156
Status: Resolved
Manufacturer: ReNew Life Formulas, Inc.
Manufactured In: United States
Units Affected: 2 products (60,781 bottles; 55,271 bottles)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.