FDA Recall United States Terminated Historical recordClass III
Nordic Naturals, Inc.
- Product
- Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gu…
- Published
- June 11, 2025
- Distribution
- Domestic: AK, AZ, CA, CO, FL, GA, ID, IN…
Nordic Naturals, Inc. Recall: Elevated levels of vitamin D3
United States
TerminatedClass II
- Company
- Nordic Naturals, Inc.
- Product
- Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3…
- Recall date
- February 7, 2024
- Terminated
- June 21, 2024
- Source
- FDA
Reason for recall
Elevated levels of vitamin D3
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3, 0.76 fl oz (22.5 mL) DIETARY SUPPLEMENT, dark glass bottle | Not published in this source record | 5564 bottles | Lot number 234909 |
Distribution
- Products are distributed to 79 consignees
- consisting of retailers
- distributors
- and consumers. Number of consignees who purchased through Amazon are unknown. U.S. distribution to AR
- AZ
- CA
- DC
- DE
- FL
- GA
- IA
- IL
- IN
- MA
- MD
- MI
- MN
- MO
- MS
- NC. ND
- NH
- NJ
- NY
- OH
- OR
- PA
- RI
- TX
- VT and WI. Additionally
- foreign customers in the Dubai and Kenya.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1109-2024
- Event ID
- 93947
- Status
- Terminated
- Classification
- Class II
- Company
- Nordic Naturals, Inc.
- Product description
- Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3, 0.76 fl oz (22.5 mL) DIETARY SUPPLEMENT, dark glass bottle
- Quantity
- 5564 bottles
- Reason
- Elevated levels of vitamin D3
- Recall initiation date
- February 7, 2024
- Report date
- April 3, 2024
- Classification date
- Not published in this source record
- Termination date
- June 21, 2024
- Distribution pattern
- Products are distributed to 79 consignees, consisting of retailers, distributors, and consumers. Number of consignees who purchased through Amazon are unknown. U.S. distribution to AR, AZ, CA, DC, DE, FL, GA, IA, IL, IN, MA, MD, MI, MN, MO, MS, NC. ND, NH, NJ, NY, OH, OR, PA, RI, TX, VT and WI. Additionally, foreign customers in the Dubai and Kenya.
- UPC, lot, and code information
- Lot number 234909
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Nordic Naturals, Inc.
Other recalls from Nordic Naturals, Inc.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| District of Columbia | 1 |
| Delaware | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New York | 1 |
| Ohio | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| Rhode Island | 1 |
| Texas | 1 |
| Vermont | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
