ANGEL branded STRAWBERRY SOFT-SERVE powder; 10- 2-pound Recall: What To Do

sks copack recall notices matter because the product involved is a food powder that families mix and serve at home. On June 10, 2026, the U.S. Food and Drug Administration published recall number 99068 involving SKS Copack. The recalled item is ANGEL branded STRAWBERRY SOFT-SERVE powder. The product may potentially be contaminated with Salmonella. The FDA classified the action as Class I, its most serious category. That classification signals a reasonable probability of serious health consequences or death.

What the Sks Copack Recall Covers

The sks copack recall covers ANGEL branded STRAWBERRY SOFT-SERVE powder. The agency record describes the packaging as 10 two-pound bags per case. The record notes there is NO UPC on the product. That detail matters for consumers. Without a UPC, you cannot scan the package to check it.

The scope listed by the FDA is 6 cases. That is a small distribution footprint. However, a small case count does not mean low risk. Each case holds ten two-pound bags. As a result, a single case can produce many individual servings once mixed and dispensed.

Soft-serve powder is typically a foodservice item. It is usually mixed with water or dairy and run through a machine. For example, it may appear at ice cream counters, snack bars, or event concessions. Some powder also reaches households through bulk retail or online sellers. The agency record does not list specific retail locations for this action.

The FDA record does not publish lot codes or best-by dates for public listing here. In most cases, that information appears in the official notice itself. Because of that, the linked FDA notice is the controlling document. Check it for any lot-level identifiers before you decide whether your product is included. View the official FDA recall notice.

The Hazard and Reported Injuries

The stated hazard is potential Salmonella contamination. Salmonella is a bacterium that causes salmonellosis. Typical symptoms include diarrhea, fever, and abdominal cramps. Symptoms usually begin six hours to six days after exposure. Most healthy adults recover within four to seven days without treatment.

However, some people face higher risk. Young children, older adults, and pregnant people are more vulnerable. So are people with weakened immune systems. In rare cases, the bacteria enter the bloodstream. That can lead to severe illness requiring hospitalization. Class I classification reflects exactly this kind of potential outcome.

Powdered products carry a particular concern. Powder does not always get cooked before serving. Soft-serve mixes are typically blended cold and dispensed cold. As a result, there is no heat step that would kill bacteria. For example, a contaminated batch served straight from a machine reaches the consumer unchanged.

The agency record does not state whether any injuries have been reported in connection with this recall. This guide does not claim that illnesses occurred, and it does not claim that none occurred. Neither statement would be supported by the record. If you believe you became ill after consuming this product, contact a healthcare provider and report it to the FDA.

What To Do If You Own This Product

Stop using the product first. Do not taste it to check whether it seems fine. Salmonella contamination has no reliable smell, color, or taste. In most cases, a contaminated batch looks completely normal. That is why identification depends on labeling, not on inspection.

Next, identify what you have. Look for the ANGEL brand name on the bag. Confirm the product is STRAWBERRY SOFT-SERVE powder. Check whether the packaging matches the 10-bag, two-pound-per-bag case format. Remember that the recalled product carries no UPC. Photograph the label and any printed codes before you take further action.

Then follow the official instructions. The remedy details in this particular agency record did not match the recalled product, so they are not repeated here. Do not assume a refund, a replacement, or a disposal instruction. Instead, follow the instructions in the official FDA notice linked on this page. That notice is the authoritative source for what to do next.

Also take a few practical safety steps. Clean any surfaces, containers, or equipment the powder touched. Wash your hands thoroughly with soap and warm water. If the product was used in a soft-serve machine, sanitize the machine per the manufacturer’s guidance. Businesses should typically document what they removed and when.

Does a Sks Copack Recall Mean You Can Sue?

A recall is not a lawsuit. That distinction is important, and it is often misunderstood. A recall is a safety action. It removes a product from the market to prevent harm. The sks copack recall is a regulatory step, not a finding of legal liability against anyone.

As a result, the existence of the sks copack recall does not by itself create a legal claim. A recall alone is not a case. In most cases, a personal injury claim requires more than a defective product. It typically requires an actual injury, and it requires causation linking that injury to the product.

For a foodborne illness claim, causation is often the hardest part. Lawyers and public health investigators typically look for documentation. That can include a medical diagnosis, laboratory confirmation of the bacteria, purchase records, and the remaining product. Timing matters too. However, none of these factors guarantee that a claim will succeed.

This article does not state that any lawsuit exists over this recall. No litigation has been verified here. If you were harmed, you may be eligible to pursue a claim. You may also not be. Only a licensed attorney reviewing your specific facts can tell you. Consult one in your state, and be aware that filing deadlines apply.

How Recalls Connect to Mass Tort Cases

Recalls sometimes become evidence in later litigation. A recall notice can document when a company learned of a problem. It can show what the company said about the defect. For example, the Philips CPAP recall in 2021 involved sound abatement foam that could degrade. That recall preceded consolidated federal litigation, and the recall record became part of the factual backdrop.

The Takata airbag inflator recalls followed a similar pattern. Those recalls grew over years and covered tens of millions of vehicles. Plaintiffs and regulators used the recall timeline to examine what was known and when. However, a recall is not proof of fault in either example. Courts still require plaintiffs to prove defect, causation, and damages under the applicable law.

Frequently Asked Questions

How do I know if my powder is part of this recall?

Look for ANGEL branded STRAWBERRY SOFT-SERVE powder in a case of ten two-pound bags. The recalled product has no UPC, so scanning will not help. Compare your packaging against the official FDA notice linked on this page.

What should I do with the product now?

Stop using it immediately and separate it from other food. The remedy instructions in the agency record did not match this product, so they are not repeated here. Follow the directions in the official FDA notice instead.

Does a Class I classification mean someone was hurt?

No. Class I describes the FDA’s assessment of potential risk, not confirmed harm. The agency record for this recall does not state whether any injuries have been reported.

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 August 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.