FDA Recall United States Terminated Historical recordClass II
D & D Foods, Inc.
- Product
- Hy-Vee, Cheese Pizza, 16'' Thin Crust, UPC 288942 611991, Ne…
- Published
- August 30, 2017
- Distribution
- The product was distributed to retail gr…
D & D Foods, Inc. Recall: Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list
United States
TerminatedClass II
- Company
- D & D Foods, Inc.
- Product
- Hy-Vee, Cheese Pizza, 12'' Thin Crust, UPC 288914 908999, Ne…
- Recall date
- July 22, 2017
- Terminated
- September 7, 2017
- Source
- FDA
Reason for recall
Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Hy-Vee, Cheese Pizza, 12'' Thin Crust, UPC 288914 908999, Net Wt. 17 oz (1 lb 1 oz) 1.06 lb (482 g), West Des Moines, IA | 288914 | 182/4 pizzas/cases | Best if Used by Dates: 04-23-2017 thru 07-26-2017 |
Distribution
- The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-3391-2017
- Event ID
- 77814
- Status
- Terminated
- Classification
- Class II
- Company
- D & D Foods, Inc.
- Product description
- Hy-Vee, Cheese Pizza, 12'' Thin Crust, UPC 288914 908999, Net Wt. 17 oz (1 lb 1 oz) 1.06 lb (482 g), West Des Moines, IA
- Quantity
- 182/4 pizzas/cases
- Reason
- Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list
- Recall initiation date
- July 22, 2017
- Report date
- August 30, 2017
- Classification date
- Not published in this source record
- Termination date
- September 7, 2017
- Distribution pattern
- The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.
- UPC, lot, and code information
- UPC 288914; Best if Used by Dates: 04-23-2017 thru 07-26-2017
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 77814 with 3 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
D & D Foods, Inc.
- Product
- Hy-Vee, Cheese Pizza, 16'' Traditional Crust, UPC 288928 611…
- Published
- August 30, 2017
- Distribution
- The product was distributed to retail gr…
FDA Recall United States Terminated Historical recordClass II
D & D Foods, Inc.
- Product
- Hy-Vee, Cheese Pizza, 12'' Traditional Crust, UPC 288900 908…
- Published
- August 30, 2017
- Distribution
- The product was distributed to retail gr…
Responsible company: D & D Foods, Inc.
Other recalls from D & D Foods, Inc.
FDA Recall United States Terminated Historical recordClass II
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- Product
- Hy-Vee Spinach, Tomato, Mozzarella Twice Baked Potatoes, Net…
- Published
- November 7, 2018
- Distribution
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FDA Recall United States Terminated Historical recordClass I
D & D Foods, Inc.
- Product
- Hy-Vee Spring Pasta Salad packaged in the following containe…
- Published
- August 15, 2018
- Distribution
- To Hy-Vee retail stores in IA, IL, KS, M…
FDA Recall United States Terminated Historical recordClass II
D & D Foods, Inc.
- Product
- Hy-Vee, Cheese Pizza, 16'' Thin Crust, UPC 288942 611991, Ne…
- Published
- August 30, 2017
- Distribution
- The product was distributed to retail gr…
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.
