PlainRecalls
FDA Food Moderate Class II Terminated

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

Reported: January 4, 2017 Initiated: September 9, 2016 #F-0906-2017

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

Reason for Recall

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

Details

Recalling Firm
Bio-Botanica, Inc.
Units Affected
a) Nature's Answer label: 93,690 bottles; b) Seeking Health label: 70,592 bottles
Distribution
Nationwide
Location
Hauppauge, NY

Frequently Asked Questions

What product was recalled?
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. Recalled by Bio-Botanica, Inc.. Units affected: a) Nature's Answer label: 93,690 bottles; b) Seeking Health label: 70,592 bottles.
Why was this product recalled?
The lots exceed the label claim for Vitamin D3 of 2000 IU per drop.
Which agency issued this recall?
This recall was issued by the FDA Food on January 4, 2017. Severity: Moderate. Recall number: F-0906-2017.