Activia Fiber Yogurt (Dannon) – Mislabeled Gluten (2016)
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
Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packaged in form fill seal plastic cups
Brand
The Dannon Company, Inc.
Lot Codes / Batch Numbers
AUG 12 2016, AUG 16 2016, AUG 19 2016, AUG 22 2016, AUG 27 2016, SEP 03 2016, SEP 08 2016, SEP 14 2106, SEP 21 2016, SEP 25 2016
Products Sold
AUG 12 2016, AUG 16 2016, AUG 19 2016, AUG 22 2016, AUG 27 2016, SEP 03 2016, SEP 08 2016, SEP 14 2106, SEP 21 2016, SEP 25 2016
The Dannon Company, Inc. is recalling Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packag due to The recalled products are incorrectly labeled because the 12 pack overwrap label includes a "Certified Gluten-Free" mark while the product contains an. 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
The recalled products are incorrectly labeled because the 12 pack overwrap label includes a "Certified Gluten-Free" mark while the product contains and the overwrap label correctly lists WHEAT as an ingredient.
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, AZ, AR, CA, FL, GA, IL, IN, KY, LA, ME, MA, MN, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI, WY, PR
Page updated: Jan 6, 2026