Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box
Summary
The FDA issued a Class II for Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box by International Food Products Corporation. Reason: Potential for Salmonella.
Details
Source
Food Recall
External ID
H-1077-2026
Action Date
2026-06-24
Status
Ongoing
Category
food
Product Description
Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box
Lot/Code Info: 5114-50, Lot 26125A6B Item number 502269 Use by 2027-05-05
Quantity Affected: 92 bags
Reason for Recall
Potential for Salmonella
Distribution
TX, TN, OK
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-18
Company
Hazelwood, MO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 47 food recalls issued in the same week, part of 204 food-related FDA actions this month.
International Food Products Corporation has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (International Food Products Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does International Food Products Corporation have FDA actions?
International Food Products Corporation has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1077-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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