PlainRecalls
FDA Food Moderate Class II Terminated

Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Sonne's Organic Foods, Inc. N. Kansas City, MO 64116; B) Springreen, No. 87, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Springreen Products, Inc. N. Kansas City, MO 64116;

Reported: March 14, 2018 Initiated: February 8, 2018 #F-0883-2018

Product Description

Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Sonne's Organic Foods, Inc. N. Kansas City, MO 64116; B) Springreen, No. 87, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Springreen Products, Inc. N. Kansas City, MO 64116;

Reason for Recall

The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.

Details

Recalling Firm
Vitalab Co Inc
Units Affected
1,703 bottles
Distribution
Product distributed to consumers, distributors and retailers in the following US states AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, NE, NJ, NY, OH, OR, PA, SD, TN, TX, UT, VA, VT, WA, WI and Canada.
Location
Kansas City, MO

Frequently Asked Questions

What product was recalled?
Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Sonne's Organic Foods, Inc. N. Kansas City, MO 64116; B) Springreen, No. 87, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Springreen Products, Inc. N. Kansas City, MO 64116;. Recalled by Vitalab Co Inc. Units affected: 1,703 bottles.
Why was this product recalled?
The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
Which agency issued this recall?
This recall was issued by the FDA Food on March 14, 2018. Severity: Moderate. Recall number: F-0883-2018.