Class IITerminatedVoluntary: Firm initiated

New Spirit Naturals Inc.: food recall H-0022-2026

New Spirit Naturals Inc. of San Dimas, CA recalled Super Muscle Support Powder; 300 grams/container UPC: NA. Reason: undeclared allergen ingredient Milk. The FDA listed it as Class II in its Enforcement Report dated Oct 15, 2025.

Record status as published: Terminated (terminated Apr 23, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Super Muscle Support Powder; 300 grams/container UPC: NA
Product quantity
178 units
Reason for recall
undeclared allergen ingredient Milk.
Codes, lots and dates on the package
Lot codes: 250312P
Distribution pattern
Products are sold directly to consumers via firm's online website.
Recalling firm
New Spirit Naturals Inc., San Dimas, CA
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Letter

Dates

EventDate
Recall initiated by the firmSep 3, 2025
Classified by the FDAOct 6, 2025
Published in the Enforcement ReportOct 15, 2025
TerminatedApr 23, 2026

Other products in the same recall event

The FDA groups related products under one recall event (event 97569).

  • H-0021-2026 — Ultra Whey Protein Powder; 1.4 lbs and 1.4 lbs. Chocolate flavor UPC: NA
  • H-0020-2026 — Gluta Plus (Glutathione) 60 capsules/container. UPC: NA
  • H-0019-2026 — Meal In A Glass protein powder. 1.05 lbs and 4.5 lbs container. UPC: NA Vanilla, Chocolate and Strawberry flavor.

All food recall records

OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.

Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0022-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.