FDA Recall United States Completed Historical recordClass II
DYMA BRANDS
- Product
- MONARCH INSTANT CHOCOLATE PUDDING & PIE FILLING MIX NATURALL…
- Published
- December 11, 2024
- Distribution
- Products were distributed to the followi…
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Policy version 2026-07-21, effective July 21, 2026.
United States
CompletedClass II
After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Sysco Classic Fruit Punch Drink Mix Natural and Artificial Flavor, NET WT. 8.6OZ (244 G), Case UPC 00734730132709, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077 | 00734730132709 | 242cs/12/8.6oz pouch | 50567: Lot 263 EFA |
This recall shares FDA event ID 95468 with 10 other product entries in Public Health Trace.
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
Responsible company: DYMA BRANDS
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed Historical recordClass II
FDA Recall United States Completed 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 |
|---|---|
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Louisiana | 1 |
| Maryland | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| Nebraska | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| West Virginia | 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 "Completed." 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.
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