Class IIITerminatedVoluntary: Firm initiated
Nordic Naturals, Inc.: food recall F-0840-2025
Nordic Naturals, Inc. of Watsonville, CA recalled Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case. Reason: Product is mislabeled. The FDA listed it as Class III in its Enforcement Report dated Jun 11, 2025; distribution: Alaska, Arizona, California, Colorado, Florida, Georgia, Idaho, Indiana, Massachusetts, Montana, North Carolina, North Dakota, New Hampshire, Nevada, New York, Oklahoma, Oregon, Rhode Island, Utah, Washington.
Record status as published: Terminated (terminated Mar 18, 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
- Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case
- Product quantity
- 1164 bottles (120 gummies/bottle)
- Reason for recall
- Product is mislabeled.
- Codes, lots and dates on the package
- Lot: 244423 RUS-30127 Expiration 05/2026
- Distribution pattern
- Domestic: AK, AZ, CA, CO, FL, GA, ID, IN, MA, MT, NC, ND, NH, NV, NY, OK, OR, RI, UT, WA; Foreign: Great Britain, UAE
- Recalling firm
- Nordic Naturals, Inc., Watsonville, CA
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 2, 2025 |
| Classified by the FDA | Jun 3, 2025 |
| Published in the Enforcement Report | Jun 11, 2025 |
| Terminated | Mar 18, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0840-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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