CLASS II Food recall · Reported 14 Sep 2016 · FDA Enforcement Report

Activia Fiber Lowfat Yogurt Strawberry/Pineapple Flavors of Cups recalled

The Dannon is recalling Activia Fiber Lowfat Yogurt Strawberry/Pineapple Flavors of Cups, distributed in 33 states. The recall was initiated on 11 Aug 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAUG 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
Quantity recalled53,545 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2099-2016
FDA event ID
74936
Recalling firm
The Dannon, Tarrytown, NY
Classification
Class II
Status
Terminated
Recall initiated
11 Aug 2016
FDA classified
8 Sep 2016
Reported
14 Sep 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Labeling Errors
Product category
Yogurt

Timeline

11 Aug 2016Recall initiated by company
8 Sep 2016Classified by FDA+28 days
14 Sep 2016Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Product as listed by the FDA

Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packaged in form fill seal plastic cups

Where it was distributed

Alabama, Arkansas, Arizona, California, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maine, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, Wyoming

AlabamaArkansasArizonaCaliforniaFloridaGeorgiaIllinoisIndianaKentuckyLouisianaMassachusettsMaineMinnesotaMissouriMississippiNorth CarolinaNebraskaNew JerseyNew MexicoNevada

Questions about this recall

Why was it recalled?

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.

Which lots are affected?

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

Where was it sold?

Alabama, Arkansas, Arizona, California, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maine, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, Wyoming

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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