Severity
Moderate
FDA Food recall · Reported September 14, 2016
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 correctl…
The Dannon Company, Inc. recalled Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 366320… - a moderate-severity action.
Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 366320… was recalled by The Dannon Company, Inc. in September 14, 2016. Reason: The recalled products are incorrectly labeled because the 12 pack overwrap label includes a "Certified Gluten…. Check the official notice for the remedy. Verify recall #F-2099-2016 with the FDA Food before acting.
The recall
The Dannon Company, Inc. issued this moderate-severity FDA Food recall-The recalled products are incorrectly labeled because the 12 pack overwrap label includes a "Certified Gluten….
Sourced from official FDA Food enforcement records. Verify recall #F-2099-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-2099-2016) was formally reported on September 14, 2016, with the manufacturer initiating the action on August 11, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. The Dannon Company, Inc. is listed as the recalling firm, operating out of Tarrytown, NY. Federal records list the affected scope as 53,545 cases.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Alabama, Arkansas, Arizona, California, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maine, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, Nevada, New Y…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
53,545 cases
Related Recalls
6
2 from same agency
Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packaged in form fill seal plastic cups
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.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2099-2016 |
| Date reported | September 14, 2016 |
| Date initiated | August 11, 2016 |
| Recalling firm | The Dannon Company, Inc. |
| Firm location | Tarrytown, NY |
| Affected scope | 53,545 cases |
| Distribution | 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,… |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 14, 2016. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.