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FDA source record Class II Terminated

Aivia Whey Protein+ Power Herbs Vanilla Bean, NET WT. 1.33 LBS (602 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street Spanish Fork, Utah 84660. UPC 0 99904...

Recall Date: 2022-07-22 Recalling Firm: NATURE'S SUNSHINE PRODUCTS Record Ref: F-1541-2022

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Aivia Whey Protein+ Power Herbs Vanilla Bean, NET WT. 1.33 LBS (602 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street Spanish Fork, Utah 84660. UPC 0 99904... and names NATURE'S SUNSHINE PRODUCTS as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: NATURE'S SUNSHINE PRODUCTS
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2022-07-22
Best identifiers to check for a FDA record

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Product Description & Identification

Aivia Whey Protein+ Power Herbs Vanilla Bean, NET WT. 1.33 LBS (602 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street Spanish Fork, Utah 84660. UPC 0 99904 22712 5 Label is read in parts: "***INGREDIENTS: Whey Isolate, Whey Concentration***".

Reason for Recall / Hazard Identified

Label declares Whey but does not declare Milk.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Nationwide.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-1541-2022
Indexed update
2026-08-09 21:59:13 UTC
Official source
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