Multi-Action Immunity Capsules (ReNew Life) – Gluten Mislabeling (2014)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle
Brand
ReNew Life Formulas, Inc.
Lot Codes / Batch Numbers
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)
Products Sold
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)
ReNew Life Formulas, Inc. is recalling PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle due to Labels indicate "no wheat" "no gluten" and the products contain gluten and wheat or a wheat related allergen.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Labels indicate "no wheat" "no gluten" and the products contain gluten and wheat or a wheat related allergen.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY, PR
Page updated: Jan 6, 2026