Recall Summary
| Recall number | H-1159-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-07-22 |
| Company | D’Dioses Fruit Pops, Inc. |
| Units affected | 149 |
| Severity | Class I |
Remedy: Follow the instructions in the official notice linked below. The agency record for this recall did not contain remedy text we could verify against this product, so we have not reproduced it here.
Read the official U.S. Food and Drug Administration recall notice
d’dioses fruit recall notices are now posted for a frozen ice pop sold in 4 oz portions. The U.S. Food and Drug Administration lists recall number H-1159-2026, dated July 22, 2026. The recalling company is D’Dioses Fruit Pops, Inc. The product is the Ice Pop, D’Dioses Fresa Leche, 4 oz (85 g), carrying UPC 710594511850. The FDA classified this action as Class I, the agency’s most serious tier. That classification matters to anyone with a food allergy in the household.
What the D’Dioses Fruit Recall Covers
The d’dioses fruit recall covers one specific frozen dessert item. It is the Ice Pop, D’Dioses Fresa Leche, packaged at 4 oz (85 g). The UPC printed on the package is 710594511850. That barcode is the single most reliable way to identify the product at home.
The agency record lists the scope as 149 units. That is a small quantity by food-recall standards. However, a limited count does not lower the risk to any one person who eats the product. In most cases, allergen recalls are judged by severity of reaction, not by volume distributed.
The FDA record for this d’dioses fruit recall does not spell out a lot code list or a full retail distribution map in the fields provided here. As a result, readers should not assume their package is safe simply because a store was not named. Typically, frozen novelty items move through distributors, small groceries, and independent retailers. Check the UPC first, then read the official notice linked on this page.
The recall date of July 22, 2026 marks the agency’s recorded action date. Product purchased before that date may still sit in a home freezer. For example, ice pops bought weeks earlier can remain frozen and edible-looking for months. That is why freezer checks matter more with frozen recalls than with fresh produce.
The Hazard and Reported Injuries
The stated hazard is undeclared ingredients. According to the FDA, the product may contain undeclared milk, pecans, pistachios, yellow #5 and red #40. Milk, pecans, and pistachios are recognized major food allergens under U.S. labeling law. Yellow #5 and red #40 are color additives that some consumers avoid or react to.
Undeclared allergens are dangerous because the label is the consumer’s only warning system. A person with a tree nut allergy reads the ingredient panel and trusts it. When pecans or pistachios are present but unlisted, that safety check fails silently. As a result, the FDA treats undeclared allergen cases with high seriousness.
A Class I classification means the FDA judged that use of the product could cause serious health consequences or death. For example, severe tree nut or milk allergy reactions can progress to anaphylaxis. Anaphylaxis can involve swelling, breathing difficulty, and a drop in blood pressure. It is a medical emergency and typically requires immediate epinephrine and a call to 911.
Whether any injuries have been reported in connection with this d’dioses fruit recall is not stated in the agency record. This guide will not claim that people were hurt. It will also not claim that nobody was hurt. Readers who want the current status should read the official FDA notice directly.
| Recall number | H-1159-2026 |
|---|---|
| Issuing agency | U.S. Food and Drug Administration |
| Recall date | July 22, 2026 |
| Company | D’Dioses Fruit Pops, Inc. |
| Product | Ice Pop, D’Dioses Fresa Leche, 4 oz (85 g), UPC 710594511850 |
| Hazard | May contain undeclared milk, pecans, pistachios, yellow #5 and red #40 |
| Units affected | 149 |
| Severity classification | Class I |
What To Do If You Own This Product
Stop eating the product now. Do not serve it to children, guests, or anyone in your care. That step applies even if nobody in the home has a known allergy. Undeclared allergens can affect people who have never had a reaction before.
Next, identify the product carefully. Look for the name D’Dioses Fresa Leche on the wrapper or box. Confirm the 4 oz (85 g) size. Then check the UPC against 710594511850. The barcode is the strongest single identifier in this d’dioses fruit recall.
The remedy instructions for this action are not restated here. The agency record contains remedy text that does not match the product, so it has been withheld from this guide. Follow the instructions in the official notice linked on this page instead. That notice is the correct source for what to do with the product itself.
If someone in your household ate the product and had a reaction, seek medical care. For severe symptoms, call 911. Save the packaging, the wrapper, and your receipt if you still have them. For example, photographs of the UPC and any lot printing can be useful later. Typically, physical evidence matters more than memory in any food safety review.
Does a D’Dioses Fruit Recall Mean You Can Sue?
A recall is not a lawsuit. It is a safety action taken by a company, often with agency oversight. The d’dioses fruit recall is a corrective step to remove product from the market. It is not a court finding, a verdict, or an admission of legal liability.
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As a result, the existence of a recall by itself does not create a legal claim for you. In most cases, a personal injury claim requires more than a defective product notice. It typically requires an actual injury and proof that the product caused it. Lawyers call that second part causation.
This guide does not state that any lawsuit has been filed over this d’dioses fruit recall. No litigation over this action has been verified here. Readers should treat any claim otherwise with caution. However, people who were genuinely harmed may still have options worth exploring.
If you or a family member suffered an allergic reaction after eating this product, you may be eligible to pursue a claim. That is a question for a licensed attorney in your state, not for a website. No outcome, payment, or settlement is promised or guaranteed here. Most consumer-injury attorneys will review the facts at no upfront charge.
How Recalls Connect to Mass Tort Cases
Recalls and mass torts are separate things that sometimes intersect. A recall notice creates a documented record. It names the product, the defect, and the date the company acted. Later, in litigation, that record can become evidence about what a company knew and when it acted.
For example, the Philips CPAP and BiPAP recall in 2021 involved sound abatement foam that could degrade. That recall was followed by consolidated federal litigation brought by users. Similarly, the Takata airbag inflator recalls became one of the largest automotive recall events in U.S. history, and related claims were litigated for years. In both examples, the recall documentation was one piece of a much larger evidentiary picture, not the case itself.
Most recalls never become mass torts. Typically, mass tort litigation forms when many people suffer similar injuries from the same product over time. A 149-unit food recall is a very different situation from a multi-million-unit device recall. However, individual injury claims can still exist even where no mass tort ever forms.
Frequently Asked Questions
How do I know if my ice pops are part of this recall?
Check the product name, the 4 oz (85 g) size, and the UPC 710594511850. The barcode is the most reliable identifier. If the UPC matches, stop eating the product and read the official FDA notice.
What does Class I mean in a food recall?
Class I is the FDA’s most serious recall classification. It means the agency judged that use of the product could cause serious health consequences or death. Undeclared allergens frequently receive this classification.
Does this recall mean I automatically have a legal case?
No. A recall is a safety action, not a lawsuit or a finding of liability. A claim generally requires an actual injury plus proof the product caused it, and only a licensed attorney can evaluate your situation.
Were You Injured by a Recalled Product?
A recall by itself is a safety action, not a legal claim. However, if a recalled product caused a real injury, you may be eligible to pursue compensation. A licensed attorney can review your situation at no upfront cost — most work on contingency, meaning you pay nothing unless you recover.
Official Sources & Resources
Verify every recall against the issuing agency before acting:
- U.S. Food and Drug Administration: official recall database — the record of truth for this notice
- CPSC: cpsc.gov — household goods, toys, furniture, appliances
- FDA: fda.gov — food, drugs, and medical devices
- NHTSA: nhtsa.gov — vehicles, tires, and child car seats
- USDA FSIS: fsis.usda.gov — meat, poultry, and egg products
Content last reviewed July 2026. This is general educational information, not legal advice. If you notice outdated information, please contact us.
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Attorney Advertising. The information on this page is provided for general informational purposes only and does not constitute legal advice. A product recall is a safety action by a manufacturer or regulator and does not by itself establish liability or create a legal claim. No attorney-client relationship is created by accessing or using this content. Every case is unique. If you believe you were harmed by a recalled product, consult a licensed attorney in your jurisdiction.