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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
An ingredient in yogurt contains soy lecithin, but soy is not declared on the label.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Strawberry Yogurt Granola Parfait packaged in clear plastic cups and labeled in the following ways: 1) Go Fresh Market Strawberry Granola Yogurt, Net wt. 6.5 oz (184 g), UPC 7 58870 32670 5, Distributed by Produce Innovation, Norwalk, IA; 2) HWY 28 Farms, Strawberry Yogurt Parfait, Net wt. 6.5 oz (184 g), UPC 7 58870 32727 6 Distributed by Produce Innovation, Norwalk, IA; 4 cups per case; 3) HWY 28 Farms, Strawberry Yogurt Parfait, Net wt. 6.5 oz (184 g); UPC 7 58870 33771 8; Distributed by Produce Innovation; 6 cups per case; 4) Your Way Fresh, Fresh Strawberry + Yogurt Parfait, Net wt. 6.25 oz (177 g), UPC 8 54426 00806 1, Distributed by Your Way Fresh LLC, Newport Beach, CA; | Not published in this source record | 1,625 cases | lot code 21229 and 21230. |
This recall shares FDA event ID 88538 with 2 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
Responsible company: Loffredo Fresh Gardens Inc. DBA Produce Innovations
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Iowa | 1 |
| Indiana | 1 |
| Missouri | 1 |
| Minnesota | 1 |
| Nebraska | 1 |
| Oklahoma | 1 |
| Texas | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
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.
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.
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.
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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