FDA recall record

Bio-Botanica Liquid VITAMIN D-3 Drops distributed under the following recall — FDA F-0906-2017

The lots exceed the label claim for Vitamin D3 of 2000 IU per drop.

Class IIclassification
F-0906-2017official record ID
Jan 4, 2017report date

Recall record at a glance

Official recordF-0906-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBio-Botanica, Inc.
Report dateJan 4, 2017
Recall initiation dateSep 9, 2016
Quantitya) Nature's Answer label: 93,690 bottles; b) Seeking Health label: 70,592 bottles
LocationHauppauge, NY, United States

Official product description

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

Why the product was recalled

The lots exceed the label claim for Vitamin D3 of 2000 IU per drop.

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.