Ultra Whey Protein Powder; 1.4 lbs and 1.4 lbs. Chocolate flavor UPC: NA
Summary
The FDA issued a Class II for Ultra Whey Protein Powder; 1.4 lbs and 1.4 lbs. Chocolate flavor UPC: NA by New Spirit Naturals Inc.. Reason: undeclared allergen ingredient Milk..
Details
Source
Food Recall
External ID
H-0021-2026
Action Date
2025-10-15
Status
Terminated
Category
food
Product Description
Ultra Whey Protein Powder; 1.4 lbs and 1.4 lbs. Chocolate flavor UPC: NA
Lot/Code Info: Lot codes: 232294P; 233634P; 240682P; 241021P; 242821P; 250201P; 251291P; 251763P; 231251P; 232303P; 233051P; 233633P; 240683P;241524P; 241582P; 242891P; 243393P; 250092P; 251041P; 251563P; 251762P
Quantity Affected: 37 units
Reason for Recall
undeclared allergen ingredient Milk.
Distribution
Products are sold directly to consumers via firm's online website.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-03
Company
San Dimas, CA
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 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.
New Spirit Naturals Inc. has 4 FDA actions in our database, including 4 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 (New Spirit Naturals Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does New Spirit Naturals Inc. have FDA actions?
New Spirit Naturals Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0021-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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