Severity
Moderate
FDA Food recall · Reported January 4, 2017
The lots exceed the label claim for Vitamin D3 of 2000 IU per drop.
Bio-Botanica, Inc. recalled Liquid VITAMIN D-3 Drops distributed under the following private labels and sizes: a) NAT… - a moderate-severity action.
Liquid VITAMIN D-3 Drops distributed under the following private labels and sizes: a) NAT… was recalled by Bio-Botanica, Inc. in January 4, 2017. Reason: The lots exceed the label claim for Vitamin D3 of 2000 IU per drop.. Check the official notice for the remedy. Verify recall #F-0906-2017 with the FDA Food before acting.
The recall
Bio-Botanica, Inc. issued this moderate-severity FDA Food recall-The lots exceed the label claim for Vitamin D3 of 2000 IU per drop..
Sourced from official FDA Food enforcement records. Verify recall #F-0906-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0906-2017) was formally reported on January 4, 2017, with the manufacturer initiating the action on September 9, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Bio-Botanica, Inc. is listed as the recalling firm, operating out of Hauppauge, NY. Federal records list the affected scope as a) Nature's Answer label: 93,690 bottles; b) Seeking Health label: 70,592 bottles.
The documented reason for this recall is: The lots exceed the label claim for Vitamin D3 of 2000 IU per drop. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
a) Nature's Answer label: 93,690 bottles; b) Seeking Health label: 70,592 bottles
Related Recalls
6
6 from same agency
Liquid VITAMIN D-3 Drops distributed under the following private labels and sizes: a) NATURE'S ANSWER VITAMIN D-3 DROPS DIETARY SUPPLEMENT, 0.5 FLUID OZ/15 mL, UPC 8300026132 -- Nature's Answer Hauppauge, NY 11788; and b) Seeking Health Optimal Vitamin D, Liquid Vitamin D-3 Drops, 2000 IU per drop, 1 FL. OZ. (30 ML), UPC 9357376983 -- Manufactured for and distributed by Seeking Health - 3140 Mercer Ave., Bellingham, WA 98225
The lots exceed the label claim for Vitamin D3 of 2000 IU per drop.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0906-2017 |
| Date reported | January 4, 2017 |
| Date initiated | September 9, 2016 |
| Recalling firm | Bio-Botanica, Inc. |
| Firm location | Hauppauge, NY |
| Affected scope | a) Nature's Answer label: 93,690 bottles; b) Seeking Health label: 70,592 bottles |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported January 4, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.