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DANONE US LLC Recall: Undeclared wheat

United States

TerminatedClass II

Company
DANONE US LLC
Product
YoCrunch¿ Vanilla Lowfat Yogurt with M&Ms 18 6oz cups per…
Recall date
April 26, 2024
Terminated
June 11, 2024
Source
FDA

Reason for recall

Undeclared wheat

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
YoCrunch¿ Vanilla Lowfat Yogurt with M&Ms 18 6oz cups per case Not published in this source record 65 cases: 18-6oz cups per case Best if Used by: June 09, 2024

Distribution

  • 1 Consignee in Florida

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1275-2024
Event ID
94538
Status
Terminated
Classification
Class II
Company
DANONE US LLC
Product description
YoCrunch¿ Vanilla Lowfat Yogurt with M&Ms 18 6oz cups per case
Quantity
65 cases: 18-6oz cups per case
Reason
Undeclared wheat
Recall initiation date
April 26, 2024
Report date
May 29, 2024
Classification date
Not published in this source record
Termination date
June 11, 2024
Distribution pattern
1 Consignee in Florida
UPC, lot, and code information
Best if Used by: June 09, 2024
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: DANONE US LLC

Other recalls from DANONE US LLC

FDA Recall United States Terminated Historical recordClass II

DANONE US LLC

Product
YoCrunch Lowfat Yogurt with Toppers Two-product package. Co…
Published
July 23, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

DANONE US LLC

Product
YoCrunch Lowfat Yogurt with Toppers. Two-product package.…
Published
July 23, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

DANONE US LLC

Product
YoCrunch Lowfat Yogurt with Toppers. Two-product packages.…
Published
July 23, 2025
Distribution
Nationwide

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.