Bountiful Trading Inc Recall: Vitamin D dietary supplement may contain Coq10
United States
TerminatedClass III
- Company
- Bountiful Trading Inc
- Product
- Kroger brand, Vitamin D3 125 mcg softgels, 100 count, Green…
- Recall date
- July 9, 2021
- Terminated
- May 19, 2022
- Source
- FDA
Reason for recall
Vitamin D dietary supplement may contain Coq10
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Kroger brand, Vitamin D3 125 mcg softgels, 100 count, Green HDPE packaging | Not published in this source record | 12,360 bottles | Prod # 19937, Lot # 508981-02, Exp 02/24 041260351211 |
Distribution
- IN
- TN
- WI
- CO
- AZ
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0789-2021
- Event ID
- 88263
- Status
- Terminated
- Classification
- Class III
- Company
- Bountiful Trading Inc
- Product description
- Kroger brand, Vitamin D3 125 mcg softgels, 100 count, Green HDPE packaging
- Quantity
- 12,360 bottles
- Reason
- Vitamin D dietary supplement may contain Coq10
- Recall initiation date
- July 9, 2021
- Report date
- July 28, 2021
- Classification date
- Not published in this source record
- Termination date
- May 19, 2022
- Distribution pattern
- IN, TN, WI, CO, AZ
- UPC, lot, and code information
- Prod # 19937, Lot # 508981-02, Exp 02/24 041260351211
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- N/A
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Bountiful Trading 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 |
|---|---|
| Indiana | 1 |
| Tennessee | 1 |
| Wisconsin | 1 |
| Colorado | 1 |
| Arizona | 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.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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.
