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

Class I - Dangerous
Recalled: December 2, 2014 ReNew Life Formulas Supplements Nationwide

What Should You Do?

  1. Check if you have this product:
    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)
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
ReNew Life Formulas, Inc.
Reason for Recall:
Labels indicate "no wheat" "no gluten" and the products contain gluten and wheat or a wheat related allergen.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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

Product Codes/Lot Numbers:

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:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1945-2015

Related Recalls