Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50
Recalled by International Food Products Corporation
Food recall
International Food Products Corporation
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
International Food Products Corporation has recalled Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on June 24, 2026 and was initiated on May 18, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, with approximately 20 bags affected. The company behind the recall is International Food Products Corporation, based in Hazelwood, MO. The FDA describes the product as: “Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, 50 lb bags”
Why was Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50 recalled?
According to the FDA, the stated reason for the recall is: “Potential for Salmonella.” In plain terms, this recall relates to Salmonella.
Salmonella is a group of bacteria that is one of the most common causes of foodborne illness in the United States. Public health authorities note that infections can lead to symptoms such as fever, diarrhea, and stomach cramps, and that young children, older adults, and people with weakened immune systems are at higher risk of serious illness. Because it can spread through contaminated food, regulators treat Salmonella findings seriously.
What should you do?
If you think you may have bought Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, compare it against the product description and identifying codes (Lot #26126A6A Use by 2027-05-06) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact International Food Products Corporation or your local health authority.
About this recall
This recall was distributed in MO. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- June 24, 2026
- Recall started
- May 18, 2026
- Distributed in
- MO
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50 recalled?+
According to the FDA: Potential for Salmonella
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-1078-2026. Information last synced from the FDA on July 5, 2026.