Five undeclared items listed at once — 32 records name more than one allergen (D'Dioses Fruit Pops)
The U.S. FDA classified "Ice Pop, D'Dioses Guayaba" (1 bar, 81.7 g) from D'Dioses Fruit Pops as Class I — its most serious category — because it may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40. Forty cases were distributed across four states.
Recall overview (primary data)
- ClassificationClass I (most serious)
- Product typeFood
- Recalling firmD'Dioses Fruit Pops, Inc.
- ReasonMay contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
- DistributionDistributed in the following states: NJ, CT, NY, PA.
- Recall initiated2026-05-04
Key points
- Recall number H-1162-2026; FDA Class I, the most serious category; status Ongoing.
- The product is "Ice Pop, D'Dioses Guayaba," 1 bar of 81.7 g, UPC 827912008432.
- The reason is that it may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40.
- Quantity 40 cases, distributed to New Jersey, Connecticut, New York, and Pennsylvania.
- Voluntary, firm-initiated. Initiated 2026-05-04; reported 2026-07-22.
- Among the FDA recall records this site holds as of 2026-09-01, 32 of the 109 undeclared-allergen records name more than one, and only this record names five.
1Five substances listed at once
The stated reason lists three allergens — milk, pecans, and pistachios — and two colors, Yellow #5 and Red #40. In the United States, milk and tree nuts (which include pecans and pistachios) are major food allergens subject to labeling, and colors must also be declared for people sensitive to them.
When this many items appear together for a single product, it suggests the label itself has fallen out of step with what is inside rather than a series of separate ingredient intrusions — though the FDA enforcement record does not state a cause.
2What kind of product an ice pop is
An ice pop can sit in a home freezer for a long time. The interval between purchase and consumption is hard to predict, which makes it likely that the product is still on hand when a recall notice appears. Other flavors from the same firm are recorded as recalled around the same time, each under its own recall number. The reliable way to check a product on hand is to match both the flavor name and the UPC (here, 827912008432).
3The reach: 40 cases across four states
The quantity is 40 cases, distributed to New Jersey, Connecticut, New York, and Pennsylvania. That is a small volume, but a Class I designation is decided by the severity of possible harm, not by how much was distributed: allergies to nuts and milk can produce severe reactions even in small amounts.
4Thirty-two records name more than one allergen
Of the 1,408 FDA recall records this site holds as of 2026-09-01, 109 cite an undeclared allergen. Sorting them by how many foods the reason names gives 41 with one, 11 with two and 20 with three; only this record names five.
Several named at once points less to a single ingredient going wrong than to a label that does not match the product at all. A single omission can sometimes be fixed by reprinting; at five, the question becomes what that label was ever a record of.
Why it matters
For a producer running several flavors on one line, a labeling mix-up propagates to multiple SKUs simultaneously. When each flavor carries its own recall number, as here, the checking burden on consumers rises, so listing both flavor and UPC in the seller notice improves effectiveness. Products kept long in a freezer are likely to still be on hand when notice goes out, which raises the importance of purchase-history notification rather than store signage alone.
FAQ
How do I tell whether a product is affected?
Why is the class the most serious when only 40 cases are involved?
Why are colors part of the recall reason?
Sources (primary)
Source: openFDA (U.S. FDA, CC0 public domain). Data is provided as-is and must not be used for medical decisions. Verify the latest and exact details with the official FDA recall information. This site is not endorsed or certified by the U.S. FDA.
- FDA recall information (official)
- openFDA (data provider)
- Recall number: H-1162-2026