Public Health Trace republishes official recall, outbreak, and surveillance data from CDC, FDA, USDA,
WHO, and other public sources. It is an independent information service, not a medical provider, and
not a substitute for professional medical advice or your local public health department's own guidance.
Policy version 2026-07-21, effective July 21, 2026.
If you are experiencing a medical emergency, call your local emergency services immediately. For food
recalls and disease investigations, always refer to the official CDC, FDA, USDA, WHO, or your local
public health authority for the most current information.
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
Recalled products
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
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
A map highlighting the states named in the source's distribution description.
Distributed
No data published
Shading reflects state-level totals only, as published by the source. It does not imply
county-level or point-level precision.
Distribution map
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.
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.